Abstract
Our recent studies on tobacco smoke carcinogen and toxicant biomarkers and cancer risk among male smokers in the Shanghai Cohort Study showed that exposure to tobacco-specific nitrosamines (TSNA) and polycyclic aromatic hydrocarbons (PAH) is prospectively associated with the risk of cancer. These findings support the hypothesis that the smokers’ cancer risk is a function of the dose of select tobacco carcinogens and highlight the importance of understanding the factors that affect the intake of these carcinogens by smokers. Given that tobacco constituent exposures are driven, at least in part, by the levels of these constituents in cigarette smoke, we measured mainstream smoke TSNA and PAH levels in 43 Chinese cigarette brands that participants of the Shanghai Cohort Study reported to smoke. In all brands analyzed here, mainstream smoke levels of NNN and NNK, the two carcinogenic TSNA, were generally relatively low, averaging (±SD) 16.8(±25.1) and 14.2(±9.5) ng/cigarette, respectively. The levels of PAH were comparable to those found in U.S. cigarettes, averaging 15(±9) ng/cigarette for benzo[a]pyrene, 119(±66) ng/cigarette for phenanthrene, and 37(±19) ng/cigarette for pyrene. Our findings indicate that the generally low levels of NNN and NNK are most likely responsible for the relatively low levels of the corresponding biomarkers in the urine of the Shanghai Cohort Study participants as compared to those found in the U.S. smokers, supporting the role of the levels of these constituents in cigarette smoke in smokers’ exposures. Our findings also suggest that, in addition to smoking, other sources contribute to Chinese smokers’ exposure to PAH.
Keywords: TSNA, PAH, nicotine, nitrate, nitrite, tobacco, smoke
Introduction
Tobacco-specific N-nitrosamines (TSNA) and polycyclic aromatic hydrocarbons (PAH) are believed to play important roles in the development of cancers associated with smoking. In laboratory animals, the carcinogenic TSNA 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and Nʹ-nitrosonornicotine (NNN) cause cancers of the lung, pancreas, oral cavity, esophagus, and nasal cavity.1,2 Many PAH are also potent carcinogens or toxicants in laboratory animals and are widely accepted as major contributors to lung cancer in smokers.3,4 Based on the extensive laboratory animal, mechanistic, and epidemiological evidence, NNN and NNK, as well as the prototypic PAH benzo[a]pyrene (BaP) are classified by the International Agency for Research on Cancer (IARC) as Group 1 carcinogens (carcinogenic to humans).1,2,4–8
Our recent studies on tobacco smoke carcinogen and toxicant biomarkers and cancer risk among male smokers in the Shanghai Cohort Study showed that the intake of TSNA and PAH is prospectively associated with the risk of cancer, providing further support for the role of these constituents in cancer development in smokers.9 Specifically, we observed a significant dose-dependent association between prospectively measured urinary total 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL), a biomarker of exposure to NNK, and the risk of lung cancer in that cohort.10 This association was also found in a prospective cohort of U.S. smokers.11 Similarly, urinary r-1,t-2,3,c-4-tetrahydroxy-1,2,3,4-tetrahydrophenanthrene (PheT), a metabolite of the non-carcinogenic PAH phenanthrene, was found to be significantly associated with lung cancer risk in the Shanghai Cohort Study.12 Phenanthrene is structurally related to the carcinogenic BaP and is always part of PAH mixtures present in various environmental sources, including cigarette smoke.13 In addition, urinary total NNN – a biomarker of exposure to NNN – was shown to be a strong predictor of esophageal cancer in smokers in the same cohort.14 All three biomarkers were independently associated with cancer risk, even after adjustment for number of cigarettes smoked per day, number of years of smoking, and nicotine intake.
The findings of the Shanghai Cohort Study strongly support the hypothesis that smokers’ cancer risk is a function of the dose of select tobacco carcinogens. Therefore, it is important to understand factors affecting the intake of these carcinogens by smokers. Tobacco constituent exposures in smokers are driven, at least in part, by the levels of these constituents in cigarette smoke. Limited studies reported that Chinese cigarettes contain relatively low levels of TSNA,15 while information on PAH content is lacking. In this study we analyzed TSNA, PAH, and nicotine in the smoke of 43 samples of Chinese cigarettes representing 40 brands smoked by the smokers in the Shanghai Cohort Study. It has been previously shown that various cigarette brands generally deliver increased amounts of PAH as TSNA levels decrease, which is suggested to be in part due to the contrasting effect of nitrate content in tobacco on TSNA formation and PAH pyrosynthesis in smoke.16,17 Therefore, we also analyzed tobacco filler TSNA, nitrate, and nitrite levels, as factors known to affect TSNA and PAH content in cigarette smoke.
Materials and Methods
Cigarettes
The cigarettes were purchased in May 2011 from four shops across a wide area of the city of Shanghai, China. Most of the common brands were manufactured in Shanghai, Beijing, Tianjin, Qingdao, and Guizhou, China. These brands were chosen based on the in-person interview results of all 1,356 male current smokers in 2010–2011 who were participants of the Shanghai Cohort Study. Among all the brands, the Double Happiness brand manufactured by the Shanghai Tobacco Co. (Shanghai, China) was most frequently smoked brand (63.3% of the Shanghai Cohort Study smokers), followed by the Daqianmen brand (7.5%).
The description of cigarette brands along with the frequencies of each brand use among the Shanghai Cohort Study smokers are summarized in Table 1. Levels of tar, nicotine, and CO printed on each pack are provided in Supplementary Table S1. Unopened sealed packs of the purchased cigarettes were stored at −20 °C until the transport to the University of Minnesota for analyses. The analyses were performed within a year from the time of their purchase.
Table 1.
No. | Brand name in Chinese |
Brand name in English (pack type and cigarette sizea) |
Additional descriptors |
Frequency of smokers in Shanghai Cohort Study (%) (n = 1356) |
---|---|---|---|---|
1 | 红双喜 | Double Happiness (HP, KS) | red/pink pack | 858 (63.27) |
2 | 红双喜 | Double Happiness (HP, KS) | red/silver pack | |
3 | 绿双喜 | Double Happiness (HP, KS) | green pack | 0 |
4 | 大前门 | DAQIANMEN (HP, KS) | silver pack | 102 (7.52) |
5 | 牡丹 | Peony (HP, KS) | red pack | 30 (2.21) |
6 | 上海牌-金色红双喜 | Double Happiness (HP, KS) | gold pack | 150 (11.06) |
7 | 中华 | Chunghwa (HP, KS) | red pack | 55 (4.06) |
8 | 三五牌 | 555-Gold Pearl (HP, KS) | white pack | 14 (1.03) |
9 | 红梅 | Hongmei (HP, KS) | orange pack | 11 (0.81) |
10 | 利群(红) | Ligun-Virginia type (HP, KS) | silver pack | 52 (3.83) |
11 | 利群(蓝) | Ligun-Virginia type (SP, KS) | gold pack | |
12 | 哈德门 | Hatamen (HP, KS) | gold pack | 5 (0.37) |
13 | 中南海(蓝) | Jhonqnanhai (HP, KS) | blue pack | 14 (1.03) |
14 | 中南海(白) | Jhonqnanhai/Five (HP, KS) | white pack | |
15 | 红河(红) | Honghe (HP, KS) | red/gold pack | 4 (0.29) |
16 | 红河(白) | Honghe (HP, KS) | white/red pack | |
17 | 黄山(红) | HuangShan (SP, KS) | red/gold pack | 9 (0.66) |
18 | 黄山(棕) | HuangShan (SP, KS) | black/red pack | |
19 | 玉溪(红) | Yuxi (SP, KS) | red dot pack | 7 (0.52) |
20 | 玉溪(棕) | Yuxi (SP, KS) | bronze pack | |
21 | 红塔山 | Hongtashan (HP, KS) | white pack | 4 (0.29) |
22 | 黄果树 | Huangguoshu (HP, KS) | red pack | 9 (0.66) |
23 | 白沙(白) | Baisha (HP, KS) | white pack | 4 (0.29) |
24 | 白沙(棕) | Baisha (SP, KS) | gold pack | |
25 | 云烟(灰) | Yun Yan/Win (HP, 95mm) | silver pack | 8 (0.59) |
26 | 云烟(红) | YunYan (HP, KS) | black/red pack | |
27 | 泰山 | Taishan (SP, KS) | rose-gold pack | 1 (0.07) |
28 | 猴王 | Houwang (HP, KS) | gold pack | 1 (0.07) |
29 | 大红鹰 | Dohongying (HP, KS) | pink/maroon pack | 3 (0.22) |
30 | 甲天下 | Fiatianxia (HP, KS) | pink stripe pack | 2 (0.15) |
31 | 五牛 | Five Bulls (HP, KS) | gold pack | 1 (0.07) |
32 | 南京(红) | NanJing (HP, KS) | red pack | 2 (0.15) |
33 | 南京(绿) | NanJing (HP, KS) | green pack | |
34 | 熊猫 | Panda (HP, KS) | orange pack | 1 (0.07) |
35 | 七星 | Mild Seven-Sky blue (HP, KS) | blue pack | 2 (0.15) |
36 | 红旗渠 | Hongqiqu (HP, KS) | red/gold pack | 1 (0.07) |
37 | 红旗渠 | Hongqiqu (SP, KS) | red pack | |
38 | 韩国ESSE | Esse Blue (HP, SS, 100mm) | white/blue pack | 2 (0.15) |
39 | 黄金叶 | Goldenleaf (HP, KS) | gold pack | 1 (0.07) |
40 | 芙蓉王 | Furongwang (HP, KS) | gold pack | 1 (0.07) |
41 | 人民大金星 | RenminDanuitang (HP, KS) | red pack | 1 (0.07) |
42 | 大卫杜夫(silver) | Davidoff Neon silver (HP, KS) | silver pack | 1 (0.07) |
43 | 大卫杜夫(supreme) | Davidoff supreme (HP, 95mm) | red pack |
HP – hard pack; SP – soft pack; KS – king size; SS – super-slim
Analyses
Cigarettes were smoked under US Federal Trade Commission (FTC) standard conditions and the mainstream smoke was collected on Cambridge filter pads as previously described.18
TSNA analyses
The four commonly analyzed TSNA – NNN, NNK, Nʹ-nitrosoanatabine (NAT) and Nʹ-nitrosoanabasine (NAB) – were analyzed by liquid chromatography (LC)-tandem mass spectrometry (MS/MS) in positive ion electrospray mode as previously described.18 Briefly, internal standards [13C6]NNN and [pyridine-D4]NNK were added to either cigarette filler samples or smoke filter pads, followed by extraction with citrate-phosphate buffer and purification of the extracts on ChemElut cartridges (Varian, Harbor City, California, USA) and Sep-Pak Plus silica cartridges (Waters, Milford, Massachusetts, USA). The purified samples were analyzed by LC-MS/MS in selected reaction monitoring mode as described.18
PAH analyses
BaP, phenanthrene, and pyrene were analyzed using our previously described gas chromatography (GC)-MS method.19 Briefly, an internal standard mix containing [13C4]BaP, [13C6]phenanthrene, and [13C6]pyrene was added to Cambridge filter pads, and the pads were extracted with hexane on a benchtop shaker for 3 hours. The extracts were purified on BondElut Silica cartridges (Varian), concentrated under a gentle stream of N2 to a final volume of 20 µL, and analyzed by GC-MS as described.19
Nicotine
Tobacco filler was extracted with methanol containing potassium hydroxide, and an aliquot of the extract was diluted with 100 mM ammonium acetate. Smoke pads were extracted with 15 mM ammonium acetate and an aliquot was diluted with 100 mM ammonium acetate. [CD3]Nicotine internal standard was used for both sample types. The prepared samples were analyzed by LC-MS/MS essentially as previously described, except that samples were eluted isocratically with acetonitrile:water:formic acid (85.6:13:1.4) containing 0.01% trifluoroacetic acid.20
Nitrate and nitrite analyses
These were analyzed essentially as previously described.21 Briefly, tobacco filler (~100mg) was extracted with deionized H2O and purified on C-18 SPE cartridges (Waters Corp., Milford, MA) prior to analysis by ion chromatography at the University of Minnesota Geochemical Analysis Facility.
Moisture content
The moisture content of cigarette filler was analyzed by a gravimetric method as previously described.22
Statistical analyses
Pearson correlations were determined using Sigma Plot 2001, v.7.101 (SPSS, Inc., Chicago, IL).
Results
The results of cigarette smoke analyses are summarized in Table 2, and the results of tobacco filler analyses are summarized in Table 3.
Table 2.
No. | Nicotine, mg/cigarette |
ng/cigarette | |||||
---|---|---|---|---|---|---|---|
Phenanthrene | Pyrene | BaP | NNN | NNK | Total TSNAa | ||
1 | 0.86 | 57 | 18 | 7 | 7.3 | 7.4 | 35.8 |
2 | 0.98 | 111 | 32 | 13 | 9.9 | 13.6 | 58.7 |
3 | 0.96 | 101 | 30 | 12 | 7.6 | 11.5 | 50.4 |
4 | 0.83 | 76 | 27 | 11 | 10.7 | 16.8 | 69.3 |
5 | 0.94 | 62 | 26 | 10 | 29.2 | 17.2 | 133.9 |
6 | 0.71 | 84 | 28 | 10 | 6.3 | 11.4 | 40.7 |
7 | 0.72 | 101 | 31 | 12 | 6.0 | 13.6 | 40.6 |
8 | 0.70 | 98 | 33 | 12 | 17.2 | 12.6 | 88.4 |
9 | 0.86 | 126 | 38 | 15 | 8.9 | 13.2 | 52.6 |
10 | 0.94 | 103 | 29 | 12 | 6.8 | 13.5 | 45.2 |
11 | 0.97 | 83 | 26 | 10 | 6.9 | 11.8 | 40.4 |
12 | 0.75 | 105 | 28 | 13 | 12.8 | 12.2 | 57.8 |
13 | 0.31 | 48 | 16 | 5 | 135.3 | 30.0 | 261.1 |
14 | 0.31 | 40 | 14 | 4 | 77.8 | 21.5 | 160.4 |
15 | 0.74 | 82 | 25 | 10 | 3.7 | 7.5 | 30.6 |
16 | 0.85 | 83 | 24 | 9 | 5.2 | 10.0 | 40.5 |
17 | 0.80 | 97 | 29 | 13 | 6.2 | 6.7 | 37.7 |
18 | 0.96 | 68 | 20 | 8 | 7.7 | 9.5 | 42.0 |
19 | 0.73 | 105 | 30 | 12 | 1.8 | 3.3 | 10.3 |
20 | 0.83 | 91 | 28 | 11 | 4.1 | 8.5 | 31.0 |
21 | 0.71 | 129 | 34 | 15 | 3.3 | 9.3 | 27.2 |
22 | 0.80 | 76 | 23 | 9 | 9.1 | 14.1 | 62.0 |
23 | 0.83 | 96 | 27 | 13 | 5.2 | 12.7 | 35.4 |
24 | 0.76 | 100 | 29 | 13 | 4.5 | 9.2 | 32.5 |
25 | 0.63 | 90 | 25 | 12 | 3.0 | 9.0 | 26.2 |
26 | 0.95 | 76 | 28 | 11 | 6.3 | 10.8 | 40.3 |
27 | 0.59 | 122 | 40 | 16 | 5.7 | 10.9 | 41.2 |
28 | 0.95 | 139 | 54 | 20 | 5.5 | 9.8 | 36.2 |
29 | 1.94 | 274 | 88 | 41 | 25.8 | 18.7 | 158.2 |
30 | 1.54 | 284 | 80 | 34 | 18.4 | 16.7 | 113.7 |
31 | 1.16 | 307 | 91 | 44 | 25.8 | 18.1 | 157.7 |
32 | 1.66 | 297 | 82 | 40 | 13.5 | 17.8 | 61.4 |
33 | 0.85 | 157 | 54 | 21 | 11.2 | 12.3 | 62.8 |
34 | 0.87 | 193 | 62 | 25 | 43.7 | 28.7 | 170.3 |
35 | 0.42 | 107 | 33 | 13 | 3.0 | 8.2 | 20.5 |
36 | 0.82 | 84 | 26 | 10 | 7.6 | 7.6 | 39.3 |
37 | 0.61 | 187 | 52 | 22 | 8.2 | 7.2 | 52.6 |
38 | 0.40 | 67 | 24 | 8 | 40.1 | 17.2 | 115.7 |
39 | 0.79 | 165 | 49 | 18 | 7.9 | 13.7 | 52.9 |
40 | 0.93 | 145 | 45 | 17 | 3.6 | 8.7 | 24.9 |
41 | 0.98 | 143 | 46 | 19 | 5.7 | 11.2 | 39.6 |
42 | 0.53 | 34 | 11 | 4 | 17.4 | 21.5 | 77.4 |
43 | 0.72 | 108 | 40 | 15 | 76.5 | 63.9 | 259.1 |
Average | 0.84 | 119 | 37 | 15 | 16.8 | 14.2 | 70.6 |
SD | 0.31 | 66 | 19 | 9 | 25.1 | 9.5 | 58.8 |
Total TSNA, sum of the four TSNA analyzed in this study: NNN, NNK, NAT, and NAB.
Table 3.
No. | Moisture, % |
mg/g (wet weight) | ug/g (wet weight) | ||||
---|---|---|---|---|---|---|---|
Nicotine | Nitrite | Nitrate | NNN | NNK | Total TSNAb | ||
1 | 14.1 | 11.9 | 0.004 | 1.0 | 0.054 | 0.058 | 0.266 |
2 | 13.8 | 15.9 | 0.021 | 3.3 | 0.070 | 0.073 | 0.319 |
3 | 12.7 | 7.9 | < 0.001 | 4.7 | 0.073 | 0.060 | 0.300 |
4 | 15.1 | 10.0 | 0.016 | 7.0 | 0.066 | 0.080 | 0.337 |
5 | 16.9 | 7.5 | 0.050 | 32.8 | 0.237 | 0.110 | 0.82 |
6 | 16.4 | 10.9 | 0.019 | 3.3 | 0.076 | 0.132 | 0.422 |
7 | 15.6 | 13.1 | < 0.001 | 0.9 | 0.054 | 0.060 | 0.258 |
8 | 15.7 | 12.4 | < 0.001 | 8.2 | 0.282 | 0.127 | 0.842 |
9 | 15.2 | 15.5 | 0.014 | 1.9 | 0.089 | 0.058 | 0.298 |
10 | 12.7 | 16.3 | 0.009 | 0.4 | 0.097 | 0.066 | 0.353 |
11 | 13.6 | 12.8 | 0.007 | 1.2 | 0.090 | 0.072 | 0.336 |
12 | 14.7 | 13.4 | < 0.001 | 2.9 | 0.113 | 0.047 | 0.356 |
13 | 14.7 | 9.6 | 0.009 | 13.3 | 1.95 | 0.171 | 2.93 |
14 | 15.0 | 10.3 | 0.016 | 14.4 | 4.67 | 0.286 | 6.38 |
15 | 13.7 | 13.2 | 0.011 | 1.8 | 0.043 | 0.071 | 0.310 |
16 | 14.1 | 13.3 | 0.011 | 1.3 | 0.036 | 0.040 | 0.232 |
17 | 14.8 | 15.5 | 0.030 | 5.5 | 0.099 | 0.060 | 0.326 |
18 | 16.6 | 17.4 | 0.027 | 0.9 | 0.118 | 0.059 | 0.341 |
19 | 15.9 | 14.9 | 0.069 | 1.1 | 0.035 | 0.053 | 0.183 |
20 | 15.4 | 15.9 | 0.019 | 2.3 | 0.041 | 0.071 | 0.228 |
21 | 15.6 | 16.3 | 0.027 | 1.4 | 0.040 | 0.042 | 0.195 |
22 | 19.0 | 16.4 | < 0.001 | 5.8 | 0.063 | 0.059 | 0.252 |
23 | 16.4 | 23.2 | 0.012 | 0.8 | 0.052 | 0.055 | 0.229 |
24 | 14.7 | 17.8 | 0.010 | 4.1 | 0.081 | 0.049 | 0.274 |
25 | 13.1 | 23.3 | 0.011 | 3.3 | 0.027 | 0.048 | 0.167 |
26 | 13.4 | 23.0 | 0.046 | 0.9 | 0.058 | 0.064 | 0.238 |
27 | 13.3 | 15.5 | 0.023 | 2.4 | 0.076 | 0.054 | 0.267 |
28 | 12.7 | 19.1 | 0.043 | 3.4 | 0.110 | 0.079 | 0.40 |
29 | 13.9 | 17.5 | 0.022 | 1.3 | 0.060 | 0.041 | 0.187 |
30 | 14.1 | 16.8 | 0.036 | 6.4 | 0.132 | 0.059 | 0.405 |
31 | 14.3 | 15.9 | 0.026 | 8.4 | 0.099 | 0.057 | 0.370 |
32 | 12.2 | 21.1 | 0.032 | 4.1 | 0.082 | 0.060 | 0.248 |
33 | 15.9 | 15.9 | < 0.001 | 3.1 | 0.131 | 0.087 | 0.418 |
34 | 13.5 | 18.7 | < 0.001 | 0.2 | 0.020 | 0.037 | 0.103 |
35 | 15.8 | 18.6 | 0.084 | 8.3 | 0.586 | 0.343 | 1.51 |
36 | 14.0 | 16.3 | 0.033 | 1.6 | 0.083 | 0.074 | 0.285 |
37 | 15.6 | 14.1 | 0.031 | 2.6 | 0.072 | 0.032 | 0.201 |
38 | 15.4 | 17.4 | 0.099 | 12.6 | 0.752 | 0.189 | 1.40 |
39 | 13.9 | 21.6 | 0.052 | 4.1 | 0.067 | 0.057 | 0.234 |
40 | 13.4 | 17.5 | 0.031 | 0.5 | 0.062 | 0.051 | 0.25 |
41 | 13.6 | 16.3 | 0.018 | 3.0 | 0.098 | 0.064 | 0.35 |
42 | 21.4 | 17.8 | 0.019 | 1.4 | 0.554 | 0.322 | 1.81 |
43 | 12.9 | 14.2 | 0.029 | 5.9 | 1.10 | 1.35 | 4.07 |
Average | 14.8 | 15.7 | 0.024 | 4.5 | 0.276 | 0.088 | 0.61 |
SD | 1.7 | 3.8 | 0.022 | 5.6 | 0.756 | 0.071 | 1.04 |
Below the limit of detection for nitrite assay (0.001 µg/g tobacco).
Total TSNA, sum of the four TSNA analyzed in this study: NNN, NNK, NAT, and NAB.
The results for cigarette smoke in Table 2 are presented on a ‘per cigarette’ basis. The levels of NNN ranged from 1.8 to 135 ng/cigarette, and the levels of NNK ranged from 3.3 to 63.9 ng/cigarette. There was also variation in the measured PAH levels, which ranged 4–44 ng/cigarette, 34–307 ng/cigarette, and 11–91 ng/cigarette, respectively, for BaP, phenanthrene, and pyrene. Nicotine levels in cigarette smoke ranged from 0.31 to 1.94 mg/cigarette.
All results for cigarette filler in Table 3 are presented per gram wet weight. Moisture content in the filler of all brands averaged 14.8±1.7% (SD). NNN levels in the filler of tested cigarettes ranged from 0.02 to 4.67 µg/g, and NNK levels ranged from 0.032 to 1.35 µg/g tobacco. Total TSNA – the sum of all four nitrosamines analyzed here – varied from 0.103 to 6.38 µg/g tobacco. The levels of nitrate and nitrite also varied widely: 0.2–32.8 mg/g tobacco for nitrate and from non-detected to 0.099 mg/g tobacco for nitrite. Nicotine levels in the filler ranged from 7.45 to 23.3 mg/g tobacco.
Relations among the tested constituents are presented in Table 4. The TSNA levels in the tobacco filler correlated with TSNA levels in cigarette smoke and with tobacco filler nitrate, but not nitrite, levels. Cigarette smoke TSNA levels also correlated with nitrate levels in tobacco filler. The negative correlation between nitrate levels in tobacco filler and PAH levels in the smoke was not statistically significant. Levels of NNN and total TSNA in tobacco filler negatively correlated with PAH levels in cigarette smoke, while negative relation between filler NNK and smoke PAH levels was not statistically significant. There was no statistically significant relation between cigarette smoke TSNA and PAH levels. Levels of various measured PAH strongly correlated with tobacco and smoke levels of nicotine and among each other. The positive correlation between nicotine levels in the tobacco filler and smoke was not significant.
Table 4.
tobacco filler | cigarette smoke | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
nicotine | nitrite | nitrate | NNN | NNK | Total TSNAa |
nicotine | phenanthrene | pyrene | BaP | NNN | NNK | ||
tobacco filler | Nitrite | r = 0.162 P = 0.23 |
|||||||||||
Nitrate | −0.441 0.0007 |
0.356 0.007 |
|||||||||||
NNN | −0.289 0.03 |
0.038 0.78 |
0.471 0.0002 |
||||||||||
NNK | −0.099 0.47 |
0.176 0.19 |
0.257 0.06 |
0.449 0.0005 |
|||||||||
Total TSNAa | −0.280 0.037 |
0.095 0.49 |
0.488 0.0001 |
0.944 <0.0001 |
0.711 <0.0001 |
||||||||
cigarette smoke | Nicotine | 0.240 0.075 |
−0.124 0.36 |
−0.210 0.12 |
−0.413 0.0016 |
−0.227 0.093 |
−0.413 0.0016 |
||||||
Phenanthrene | 0.353 0.0076 |
0.037 0.79 |
−0.184 0.17 |
−0.276 0.039 |
−0.148 0.28 |
−0.285 0.033 |
0.731 <0.0001 |
||||||
Pyrene | 0.338 0.011 |
0.092 0.50 |
−0.136 0.32 |
−0.265 0.048 |
−0.106 0.44 |
−0.263 0.050 |
0.725 <0.0001 |
0.972 <0.0001 |
|||||
BaP | 0.317 0.017 |
0.029 0.83 |
−0.144 0.29 |
−0.267 0.047 |
−0.138 0.31 |
−0.272 0.043 |
0.749 <0.0001 |
0.958 <0.0001 |
0.965 <0.0001 |
||||
NNN | −0.291 0.029 |
0.065 0.63 |
0.523 <0.0001 |
0.746 <0.0001 |
0.581 <0.0001 |
0.806 <0.0001 |
−0.259 0.054 |
−0.123 0.37 |
−0.099 0.47 |
−0.103 0.45 |
|||
NNK | −0.109 0.42 |
0.097 0.48 |
0.347 0.009 |
0.490 0.0001 |
0.829 <0.0001 |
0.695 <0.0001 |
−0.049 0.72 |
0.029 0.83 |
0.055 0.69 |
0.048 0.73 |
0.807 <0.0001 |
||
Total TSNAa | −0.233 0.084 |
0.123 0.37 |
0.513 <0.0001 |
0.586 <0.0001 |
0.633 <0.0001 |
0.707 <0.0001 |
−0.041 0.76 |
0.067 0.62 |
0.098 0.47 |
0.104 0.44 |
0.922 <0.0001 |
0.912 <0.0001 |
Total TSNA, sum of the four TSNA analyzed in this study: NNN, NNK, NAT, and NAB.
Discussion
Tobacco constituent intake in smokers can be affected by a variety of factors, including the levels of the constituents in cigarette smoke, individual smoking topography, and other individual characteristics of smokers. To provide insights into the potential contribution of cigarette smoke content to carcinogen intake by smokers in the Shanghai Cohort Study, we analyzed TSNA and PAH – the pertinent carcinogens – in cigarette brands smoked by the cohort participants. This is the first study to characterize multiple constituents in both the tobacco filler and the smoke of a wide range of Chinese cigarette brands.
The levels of TSNA in the smoke of cigarettes analyzed in this study were generally relatively low, in the range that is typically associated with Virginia tobacco.23 A histogram showing the distribution of smoke TSNA levels in the brands analyzed here is illustrated in Figure 1A. It demonstrates that, while some of the analyzed brands contained higher levels of NNN and NNK, the sum of these carcinogens in the smoke of 88% of the brands is less than 50 ng/cigarette. These results are consistent with the levels reported in a previous study that examined the smoke of 39 unspecified Chinese cigarette brands.15 For comparison, we recently reported that the sum of NNN and NNK in U.S. cigarettes ranged from 45 to 366 ng/cigarette, with 16 out of 17 brands containing these constituents at levels higher than 100 ng/cigarette.18 The range of PAH levels measured in this study was similar to that reported for US cigarettes,2,24,25 with 93% of the tested brands containing BaP at levels below 30 ng/cigarette (Figure 1B). These results are in agreement with the limited available data for Chinese cigarettes.26 On the other hand, these results are in contrast with the general expectation that lower levels of TSNA in cigarette smoke are necessarily accompanied by increases in PAH levels, which is based in part on the contrasting effect of nitrate content in tobacco on TSNA formation and PAH pyrosynthesis in smoke Nitrate is the source of nitrosating species that react with tobacco alkaloids producing TSNA, and it has been shown that TSNA levels in tobacco products depend on tobacco nitrate content.23,27,28 At the same time, higher nitrate content generates higher amounts of nitrogen oxides during tobacco combustion, and these oxides ‘capture’ and neutralize some radicals that otherwise could form PAH.29 Indeed, it has been previously reported that various cigarette brands generally delivered increased amounts of PAH as TSNA levels decreased.17 However, brand-by-brand examination of an international sample of cigarettes for which an overall negative correlation between TSNA and PAH was observed shows that many individual brands do not follow this pattern.17 In the present study, TSNA levels in both tobacco filler and cigarette smoke correlated with nitrate levels in tobacco (Table 4). We also observed a slight negative correlation between tobacco nitrate levels and the smoke PAH yields (Table 4). However, there was no significant relationship between BaP and the sum of NNN and NNK in the smoke (Figure 2). These findings suggest that TSNA levels in cigarette smoke can be reduced without necessarily increasing PAH levels in the smoke of the same cigarettes. Furthermore, TSNA levels in cigarette smoke strongly correlated with those in the tobacco filler, consistent with previous findings that the levels of preformed TSNA in tobacco determine yields in smoke.2,16,18,30 Together, these observations support the importance of tobacco processing and blending approaches which could be modified to reduce smoke TSNA exposures.31
The results of this study help to provide insights into the contribution of cigarette smoke TSNA and PAH content to the biomarker-assessed exposure to these carcinogens in smokers in the Shanghai Cohort Study. For instance, our previous research showed that urinary levels of TSNA biomarkers were lower, and those of PAH higher, in the smokers from the Shanghai Cohort Study as compared to the levels of corresponding biomarkers typically reported for U.S. smokers. Urinary total NNN averaged 0.06 pmol/mg creatinine14 and total NNAL averaged 0.20 pmol/mg creatinine12 in the Shanghai Cohort Study smokers, while in U.S. smokers these levels are 0.14 pmol/mg creatinine32 and approximately 1.0−1.5 pmol/mg creatinine,33,34 respectively. More than 95% of smokers in the Shanghai Cohort Study smoked cigarette brands containing the sum of NNN and NNK at levels below 30 ng/cigarette (see Tables 1 and 2). Taken together, our findings suggest that lower NNN and NNK levels in mainstream smoke of cigarette brands used by smokers in the Shanghai Cohort Study are most likely responsible for the lower urinary levels of total NNN and total NNAL in these smokers as compared to the levels typically measured in U.S. smokers. This is in agreement with a previous report showing that smokers of cigarettes with lower NNK content have in their urine lower levels of NNAL as compared to smokers of high-NNK cigarettes.35 In contrast, urinary PheT in the Shanghai Cohort Study averaged 28.1 pmol/mg creatinine (95% confidence interval, 26.7−29.5),12 or approximately 10-fold higher than the levels of this biomarker in U.S. smokers (ranging from 3.7 to 5 pmol/mg creatinine).36–38 Given that smoke PAH levels measured in this study are similar to those found in the U.S. cigarettes, and that PAH are ubiquitous environmental contaminants, it is likely that exposures from other sources, for instance air pollution, diet, or occupational exposures contributed to the high levels of PAH exposure in the Shanghai Cohort Study smokers. In support of this hypothesis, considerably higher levels of PheT were also observed in Chinese non-smokers as compared to non-smokers from the US.39
In summary, we analyzed TSNA and PAH in cigarette brands that were used by smokers in the Shanghai Cohort Study. Our findings support the role of NNN and NNK content in cigarette smoke as an important factor influencing the exposures to these carcinogens in smokers. The results of PAH analyses suggest that the high levels of PAH biomarkers measured in the Shanghai Cohort Study are substantially affected by factors other than the levels of these constituents in Chinese cigarettes. While these findings do not undermine the importance of the association between urinary PheT and lung cancer risk in the Shanghai Cohort smokers, further research is needed to understand the major factors affecting PAH intake and the subsequent risk of lung cancer in this cohort.
Supplementary Material
Novelty and Impact.
Biomarker-assessed levels of exposure to carcinogenic tobacco-specific N-nitrosamines (TSNA) and polycyclic aromatic hydrocarbons (PAH) have been associated with the risk of lung cancer in smokers from the Shanghai Cohort Study. Understanding the factors contributing to these exposures could provide critical insights for the development of preventive measures. We examined the levels of TSNA and PAH in Chinese cigarette brands that were smoked by the Shanghai Cohort Study participants. This is the first study to characterize multiple constituents in both the smoke and the tobacco filler of a wide range of Chinese cigarette brands. The results indicate that smoke TSNA content play an important role in smokers’ exposures to these constituents, while additional sources of exposure most likely contributed significantly to PAH intake among the Shanghai Cohort Study smokers.
Acknowledgments
We thank Ms. Yue-Li Wang of the Shanghai Cancer Institute and Dr. Bin Ma for help with purchasing and characterizing cigarettes, Dr. Peter Villalta for help with mass-spectrometry, and Dr. Linda VonWeymarn for help with nicotine assay. We also thank Bob Carlson for editorial assistance. This study was supported by grants no. CA-129534, CA-144034, and CA-81301 from the National Cancer Institute, and startup funds to IS from the Masonic Cancer Center.
Reference List
- 1.Hecht SS. Tobacco carcinogens, their biomarkers, and tobacco-induced cancer. Nature Rev Cancer. 2003;3:733–744. doi: 10.1038/nrc1190. [DOI] [PubMed] [Google Scholar]
- 2.IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. Vol. 83. Lyon, FR: IARC; 2004. International Agency for Research on Cancer, Tobacco Smoke and Involuntary Smoking. [PMC free article] [PubMed] [Google Scholar]
- 3.Ding YS, Ashley DL, Watson CH. Determination of 10 carcinogenic polycyclic aromatic hydrocarbons in mainstream cigarette smoke. J Agric Food Chem. 2007;55:5966–5973. doi: 10.1021/jf070649o. [DOI] [PubMed] [Google Scholar]
- 4.IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. Vol. 92. Lyon, FR: IARC; 2010. International Agency for Research on Cancer, Some Non-Heterocyclic Polycyclic Aromatic Hydrocarbons and Some Related Exposures; pp. 35–818. [PMC free article] [PubMed] [Google Scholar]
- 5.Hecht SS. Biochemistry, biology, and carcinogenicity of tobacco-specific N-nitrosamines. Chem Res Toxicol. 1998;11:559–603. doi: 10.1021/tx980005y. [DOI] [PubMed] [Google Scholar]
- 6.IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. Vol. 89. Lyon, FR: IARC; 2007. International Agency for Research on Cancer, Smokeless tobacco and some tobacco-specific N-nitrosamines. [PMC free article] [PubMed] [Google Scholar]
- 7.Pfeifer GP, Denissenko MF, Olivier M, Tretyakova N, Hecht SS, Hainaut P. Tobacco smoke carcinogens, DNA damage and p53 mutations in smoking-associated cancers. Oncogene. 2002;21:7435–7451. doi: 10.1038/sj.onc.1205803. [DOI] [PubMed] [Google Scholar]
- 8.Hecht SS. Tobacco smoke carcinogens and lung cancer. J Natl Cancer Inst. 1999;91:1194–1210. doi: 10.1093/jnci/91.14.1194. [DOI] [PubMed] [Google Scholar]
- 9.Hecht SS, Murphy SE, Stepanov I, Nelson HH, Yuan JM. Tobacco smoke biomarkers and cancer risk among male smokers in the Shanghai Cohort Study. Cancer Lett. 2012;334:34–38. doi: 10.1016/j.canlet.2012.07.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Yuan JM, Koh WP, Murphy SE, Fan Y, Wang R, Carmella SG, Han S, Wickham K, Gao YT, Yu MC, Hecht SS. Urinary levels of tobacco-specific nitrosamine metabolites in relation to lung cancer development in two prospective cohorts of cigarette smokers. Cancer Res. 2009;69:2990–2995. doi: 10.1158/0008-5472.CAN-08-4330. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Church TR, Anderson KE, Caporaso NE, Geisser MS, Le CT, Zhang Y, Benoit AR, Carmella SG, Hecht SS. A prospectively measured serum biomarker for a tobacco-specific carcinogen and lung cancer in smokers. Cancer Epidemiol Biomarkers Prev. 2009;18(1):260–266. doi: 10.1158/1055-9965.EPI-08-0718. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Yuan JM, Gao YT, Murphy SE, Carmella SG, Wang R, Zhong Y, Moy KA, Davis AB, Tao L, Chen M, Han S, Nelson HH, et al. Urinary levels of cigarette smoke constituent metabolites are prospectively associated with lung cancer development in smokers. Cancer Res. 2011;71(21):6749–6757. doi: 10.1158/0008-5472.CAN-11-0209. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Hecht SS, Carmella SG, Villalta PW, Hochalter JB. Analysis of phenanthrene and benzo[a]pyrene tetraol enantiomers in human urine: relevance to the bay region diol epoxide hypothesis of benzo[a]pyrene carcinogenesis and to biomarker studies. Chem Res Toxicol. 2010;23:900–908. doi: 10.1021/tx9004538. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Yuan JM, Knezevich AD, Wang R, Gao YT, Hecht SS, Stepanov I. Urinary levels of the tobacco-specific carcinogen N'-nitrosonornicotine and its glucuronide are strongly associated with esophageal cancer risk in smokers. Carcinogenesis. 2011;32(9):1366–1371. doi: 10.1093/carcin/bgr125. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Xiong W, Hou H, Jiang X, Tang G, Hu Q. Simultaneous determination of four tobacco-specific N-nitrosamines in mainstream smoke for Chinese Virginia cigarettes by liquid chromatography-tandem mass spectrometry and validation under ISO and "Canadian intense" machine smoking regimes. Anal Chim Acta. 2010;674(1):71–78. doi: 10.1016/j.aca.2010.06.011. [DOI] [PubMed] [Google Scholar]
- 16.Wu W, Zhang L, Jain RB, Ashley DL, Watson CH. Determination of carcinogenic tobacco-specific nitrosamines in mainstream smoke from U.S.-brand and non-U.S.-brand cigarettes from 14 countries. Nicotine Tob Res. 2005;7(3):443–451. doi: 10.1080/14622200500125898. [DOI] [PubMed] [Google Scholar]
- 17.Ding YS, Yan XJ, Jain RB, Lopp E, Tavakoli A, Polzin GM, Stanfill SB, Ashley DL, Watson CH. Determination of 14 polycyclic aromatic hydrocarbons in mainstream smoke from U.S. brand and non-U.S. brand cigarettes. Environ Sci Technol. 2006;40(4):1133–1138. doi: 10.1021/es0517320. [DOI] [PubMed] [Google Scholar]
- 18.Stepanov I, Knezevich A, Zhang L, Watson CH, Hatsukami DK, Hecht SS. Carcinogenic tobacco-specific N-nitrosamines in US cigarettes: three decades of remarkable neglect by the tobacco industry. Tobacco Control. 2012;21:44–48. doi: 10.1136/tc.2010.042192. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Stepanov I, Villalta PW, Knezevich A, Jensen J, Hatsukami DK, Hecht SS. Analysis of 23 polycyclic aromatic hydrocarbons in smokeless tobacco by gas chromatography-mass spectrometry. Chem Res Toxicol. 2010;23:66–73. doi: 10.1021/tx900281u. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Murphy SE, Villalta P, Ho SW, von Weymarn LB. Analysis of [3',3'-d(2)]-nicotine and [3',3'-d(2)]-cotinine by capillary liquid chromatography-electrospray tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci. 2007;857:1–8. doi: 10.1016/j.jchromb.2007.06.018. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Stepanov I, Hecht SS, Ramakrishnan S, Gupta PC. Tobacco-specific nitrosamines in smokeless tobacco products marketed in India. Intl J Cancer. 2005;116:16–19. doi: 10.1002/ijc.20966. [DOI] [PubMed] [Google Scholar]
- 22.Stepanov I, Jensen J, Hatsukami D, Hecht SS. New and traditional smokeless tobacco: comparison of toxicant and carcinogen levels. Nicotine Tob Res. 2008;10(12):1773–1782. doi: 10.1080/14622200802443544. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Hoffmann D, Adams JD, Brunnemann KD, Hecht SS. Assessment of tobacco-specific N-nitrosamines in tobacco products. Cancer Res. 1979;39:2505–2509. [PubMed] [Google Scholar]
- 24.Borgerding MF, Bodnar JA, Wingate DE. A Research Study Conducted after Consultation with the Massachusetts. Department of Public Health; 2000. The 1999 Massachusetts Benchmark Study - Final report. [ http://www.brownandwilliamson.com/APPS/PDF/Final_Report_1999_Mass_Benchmark_Study pdf] [Google Scholar]
- 25.Counts ME, Hsu FS, Laffoon SW, Dwyer RW, Cox RH. Mainstream smoke constituent yields and predicting relationships from a worldwide market sample of cigarette brands: ISO smoking conditions. Regul Toxicol Pharmacol. 2004;39:111–134. doi: 10.1016/j.yrtph.2003.12.005. [DOI] [PubMed] [Google Scholar]
- 26.Akpan V, Huang S, Lodovici M, Dolara P. High levels of carcinogenic polycyclic aromatic hydrocarbons (PAH) in 20 brands of Chinese cigarettes. J Appl Toxicol. 2006;26(6):480–483. doi: 10.1002/jat.1165. [DOI] [PubMed] [Google Scholar]
- 27.Hoffmann D, Hecht SS, Ornaf RM, Wynder EL, Tso TC. Nitrosonornicotine: presence in tobacco, formation and carcinogenicity. In: Walker EA, Bogovski P, Griciute L, editors. Environmental N-Nitroso Compounds: Analysis and Formation. Lyon, France: International Agency for Research on Cancer; 1976. pp. 307–320. [Google Scholar]
- 28.Hecht SS, Chen CB, Dong M, Ornaf RM, Hoffmann D, Tso TC. Studies on non-volatile nitrosamines in tobacco. Beitr Tabakforsch Int. 1977;9:1–6. [Google Scholar]
- 29.Ding YS, Zhang L, Jain RB, Jain N, Wang RY, Ashley DL, Watson CH. Levels of tobacco-specific nitrosamines and polycyclic aromatic hydrocarbons in mainstream smoke from different tobacco varieties. Cancer Epidemiol Biomarkers Prev. 2008;17(12):3366–3371. doi: 10.1158/1055-9965.EPI-08-0320. [DOI] [PubMed] [Google Scholar]
- 30.Fischer S, Spiegelhalder B, Eisenbarth J, Preussmann R. Investigations on the origin of tobacco-specific nitrosamines in mainstream smoke of cigarettes. Carcinogenesis. 1990;11:723–730. doi: 10.1093/carcin/11.5.723. [DOI] [PubMed] [Google Scholar]
- 31.Hecht SS. It is time to regulate carcinogenic tobacco-specific nitrosamines in cigarette tobacco. Cancer Prevention Research. 2014;7:639–647. doi: 10.1158/1940-6207.CAPR-14-0095. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Stepanov I, Carmella SG, Briggs A, Hertsgaard L, Lindgren B, Hatsukami D, Hecht SS. Presence of the carcinogen N'-nitrosonornicotine in the urine of some users of oral nicotine replacement therapy products. Cancer Res. 2009;69(21):8236–8240. doi: 10.1158/0008-5472.CAN-09-1084. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Hatsukami DK, Kotlyar M, Hertsgaard LA, Zhang Y, Carmella SG, Jensen JA, Shields PG, Murphy SE, Stepanov I, Hecht SS. Reduced nicotine content cigarettes: effects on toxicant exposure, dependence and cessation. Addiction. 2010;105:343–355. doi: 10.1111/j.1360-0443.2009.02780.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Kotlyar M, Hertsgaard LA, Lindgren BR, Jensen JA, Carmella SG, Stepanov I, Murphy SE, Hecht SS, Hatsukami DK. Effect of oral snus and medicinal nicotine in smokers on toxicant exposure and withdrawal symptoms: a feasibility study. Cancer Epidemiol Biomarkers & Prev. 2011;20(1):91–100. doi: 10.1158/1055-9965.EPI-10-0349. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Ashley DL, O'Connor RJ, Bernert JT, Watson CH, Polzin GM, Jain RB, Hammond D, Hatsukami DK, Giovino GA, Cummings KM, McNeill A, Shahab L, et al. Effect of differing levels of tobacco-specific nitrosamines in cigarette smoke on the levels of biomarkers in smokers. Cancer Epidemiol Biomarkers & Prev. 2010;19(6):1389–1398. doi: 10.1158/1055-9965.EPI-10-0084. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Hecht SS, Chen M, Yagi H, Jerina DM, Carmella SG. r-1,t-2,3,c-4-Tetrahydroxy-1,2,3,4-tetrahydrophenanthrene in human urine: a potential biomarker for assessing polycyclic aromatic hydrocarbon metabolic activation. Cancer Epidemiol Biomarkers & Prev. 2003;12:1501–1508. [PubMed] [Google Scholar]
- 37.Hecht SS, Chen M, Yoder A, Jensen J, Hatsukami D, Le C, Carmella SG. Longitudinal study of urinary phenanthrene metabolite ratios: effect of smoking on the diol epoxide pathway. Cancer Epidemiol Biomarkers & Prev. 2005;14(12):2969–2974. doi: 10.1158/1055-9965.EPI-05-0396. [DOI] [PubMed] [Google Scholar]
- 38.Hecht SS, Carmella SG, Yoder A, Chen M, Li Z, Le C, Jensen J, Hatsukami DK. Comparison of polymorphisms in genes involved in polycyclic aromatic hydrocarbon metabolism with urinary phenanthrene metabolite ratios in smokers. Cancer Epidemiol Biomarkers & Prev. 2006;15:1805–1811. doi: 10.1158/1055-9965.EPI-06-0173. [DOI] [PubMed] [Google Scholar]
- 39.Kensler TW, Ng D, Carmella SG, Chen M, Jacobson LP, Munoz A, Egner PA, Chen JG, Qian GS, Chen TY, Fahey JW, Talalay P, et al. Modulation of the metabolism of airborne pollutants by glucoraphanin-rich and sulforaphane-rich broccoli sprout beverages in Qidong, China. Carcinogenesis. 2012;33(1):101–107. doi: 10.1093/carcin/bgr229. [DOI] [PMC free article] [PubMed] [Google Scholar]
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