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Journal of Experimental & Clinical Cancer Research : CR logoLink to Journal of Experimental & Clinical Cancer Research : CR
. 2012 Dec 12;31(1):101. doi: 10.1186/1756-9966-31-101

Alpha B-crystallin is a new prognostic marker for laryngeal squamous cell carcinoma

Yuan Mao 1,#, Da-Wei Zhang 2,#, Hong Lin 3, Lin Xiong 4, Ying Liu 1, Qing-Dong Li 1, Jun Ma 5, Qing Cao 2, Ren-Jie Chen 2,✉, Jin Zhu 6,7,✉, Zhen-Qing Feng 6
PMCID: PMC3551651  PMID: 23231769

Abstract

Background

Alpha B-crystallin (αB-crystallin) has been suggested to play an important role in the development of solid tumors. However, the association between αB-crystallin expression and clinicopathological characteristics of human laryngeal carcinoma is not well defined. This study aimed to examine the expression of αB-crystallin in human laryngeal squamous cell carcinoma (LSCC) and investigate the relationship between its expression and the prognosis of LSCC.

Methods

Real-time polymerase chain reaction (six LSCC samples, six tumor-adjacent normal samples) and immunohistochemistry by tissue microarrays (109 LSCC samples and 28 tumor-adjacent normal samples) were performed to characterize expression of the αB-crystallin gene in LSCC. Kaplan-Meier survival and Cox regression analyses were carried out to evaluate the prognosis of LSCC.

Results

Real-time polymerase chain reaction and immunohistochemistry analysis showed that the expression of αB-crystallin in LSCC was significantly higher than that in tumor-adjacent normal tissues. Moreover, the expression level of αB-crystallin protein in LSCC was significantly related to alcohol consumption (P = 0.022), tumor differentiation (P = 0.007), pTNM stage (P = 0.041) and 5 years’ survival (P =0.030). COX multi-factor analysis showed that αB-crystallin (P = 0.013), as well as pTNM stage (P =0.027) and lymphatic metastasis (P = 0.015) were independent prognosis factors for LSCC.

Conclusions

The data suggest that αB-crystallin expression is correlated with malignant phenotypes of LSCC and it may serve as a novel prognostic factor for LSCC.

Keywords: Laryngeal carcinoma, Alpha B-crystallin gene, RT-PCR, qPCR, Immunohistochemistry, Prognosis

Introduction

Squamous cell carcinoma (SCC) of the head and neck is one of the most frequent malignancies in the world, with about a quarter of all cases occurring in the developing countries. SCC accounts for nearly 90% of all head and neck carcinomas [1]. Approximately, one-fourth of all head and neck cancers are laryngeal squamous cell carcinoma (LSCC). LSCC is a malignant tumor of laryngeal epithelial origin and the clinical symptoms usually depend on its original site and size [2,3]. Although several cutting-edge treatment strategies have been developed for LSCC, no treatment could achieve a satisfactory therapeutic outcome and the mortality rate of LSCC is still high (5-year survival rate is 64%) [4]. Therefore, it is urgent to develop novel and valuable markers to distinguish patients with poor prognosis or at high risk of early recurrence and guide chemotherapy and radiotherapy [5].

Alpha B-crystallin (αB-crystallin) is a member of the small heat shock protein (sHSP) family and acts as a molecular chaperone, by preventing the aggregation of denatured proteins after the exposure to stresses such as heat shock, radiation, oxidative stress and anticancer drugs [6]. Moreover, ectopic expression of αB-crystallin in diverse cell types confers protection against a variety of apoptotic stimuli, including TNF-α, TNF-related apoptosis-inducing ligand (TRAIL), etoposide and growth factor deprivation [7,8]. It is believed that αB-crystallin can interact with different apoptotic proteins to regulate apoptosis [9]. Recent studies suggest that αB-crystallin is a prognostic marker for various types of solid tumors [10-12]. αB-crystallin may play a role in tumorigenesis by modulating vascular endothelial growth factor (VEGF) [13,14]. However, the expression and function of αB-crystallin in LSCC have not been determined.

In this study, we examined the expression levels of αB-crystallin in LSCC tissues and tumor-adjacent normal tissues. The results showed that compared to tumor-adjacent normal tissues, αB-crystallin expression was higher in LSCC tissues. In addition, αB-crystallin expression in LSCC was associated with alcohol consumption, tumor differentiation, pTNM stage and 5-year survival.

Materials and methods

Patient specimens

A total of one hundred and nine cases of LSCC were collected from the Department of Pathology, the Affiliated Hospital of Nantong University between 2000 and 2009. Diagnosis of LSCC was determined according to the latest WHO criteria [15] and TNM stage classification (UICC 2002). Among the cases, there were 107 men and 2 women. The mean age of patients at the time of surgery was 60.8 years (ranging from 29 to 87 years). Related clinical data were collected, including gender, age, tobacco and alcohol consumption, tumor differentiation, pTNM stage, lymph node metastasis, and 5-year follow-up survival. Follow-up in all patients started from post-operation of May 2010. None of the 109 patients had performed radiotherapy, chemotherapy or immunotherapy before the surgery. Study protocol was approved by the Ethics Committee of Jiangsu Province Official Hospital.

Reverse transcription-polymerase chain reaction (RT-PCR) and quantitative real-time polymerase chain reaction analysis (qPCR)

Six samples of fresh LSCC tissues and their adjacent tissues were collected from the Department of Otolaryngology-Head and Neck Surgery, the Second Affiliated Hospital of Nanjing Medical University and the Department of Otolaryngology-Head and Neck Surgery, Yiji Shan Hospital of Wannan Medical College. Total RNA was extracted from LSCC tissues and tumor-adjacent tissues by using Trizol reagent (Invitrogen, Carlsbad, CA) according to the manufacturer's protocol. RNA (2 μg) was reverse transcribed using High-Capacity cDNA Archive Kit (Promega) in accordance with the manufacturer's protocols. Primers were as follows: αB-crystallin forward 5’-CTTTGACCAGTTCTTCGGAG-3’, reverse 5’-CCTCAATCACATCTCCCAAC-3’; β-actin forward 5’- CTCCATCCTGGCCTCGCTGT-3’, reverse 5’- GCTGCTACCTTCACCGTTCC-3’. The transcription levels of β-actin served as a loading control. Analysis of qPCR was performed using SYBR green dye in an ABI PRISM 7000HT Sequence Detection System (Applied Biosystems, Foster City, CA, USA) following the manufacturer’s instructions. Cycle conditions were as follows: after an initial incubation at 50°C for 2-min and at 95°C for 10 min, the samples were cycled 40 times at 95°C for 15 seconds and 56°C for 1 min.

Tissue microarrays (TMA) construction and immunohistochemistry

Formalin-fixed, paraffin-embedded tissues from 109 LSCC and 28 tumor-adjacent normal tissues were prepared and utilized in this present study. TMA was produced by Xinchao Biotech (Shanghai, China). Core tissue biopsies (2 mm in diameter) were taken from individual paraffin-embedded LSCC and arranged in the new recipient paraffin blocks. Tissue microarray was cut into 4-μm sections and placed on super frost charged glass microscope slides.

Paraffin tissue sections (4 μm) were deparaffinized in 100% xylene and re-hydrated in descending ethanol series and water according to standard protocols. Heat-induced antigen retrieval was performed in 10 mM citrate buffer for 2 min at 100°C. Endogenous peroxidase activity was blocked by hydrogen peroxidase (3%) in Tris-buffered saline (TBS) for 30 min. Then the sections were boiled for 10 min in citrate buffer for antigen retrieval. Nonspecific binding was blocked by incubation with 5% goat serum in TBS for 30 min. Tissue sections were incubated with mouse anti-αB-crystallin antibody (Stressgen, Victoria, Canada; 1:300) in TBS containing 1% bovine serum albumin for 1 h. After washing, sections were incubated with EnVision goat anti-mouse/horseradish peroxidase antibody (EB-2305, ZhongShan, Godbridge, China; 1:2000) for 1 h. The replacement of the primary antibody with PBS served as negative controls. Finally, the sections were developed with 3,3-diaminobenzidine (DAB) chromogen solution and counterstained with hematoxylin. Four fields in each slide were randomly selected and counted, and the percentage of positive staining was determined by two clinical pathologists independently using immunohistochemistry score (IHS) [16]. When a conclusion differed, the final decision was made by consensus. The results were analyzed according to the method described previously [17]. Briefly, IHS was determined by the evaluation of both staining density and intensity. The percentage of positive tumor cells was scored as follows: 1 (0-10% positive cells), 2 (11-50% positive cells), 3 (51-80% positive cells), 4 (81-100% positive cells); and the intensity of staining was scored as follows: 0 (negative), 1 (weakly positive), 2 (moderately positive), and 3 (strongly positive). Multiplication of the intensity and the percentage scores gave rise to the ultimate IHS: a sum score below 3 indicated low expression of αB-crystallin, and a sum score above 4 indicated high expression of αB-crystallin.

Statistical analysis

The relationship between αB-crystallin expression and clinicopathological factors was analyzed by chi-square test. Survival rate was estimated by Kaplan-Meier method. Univariate and multivariate analysis was carried out using Cox’s proportional hazards regression models. For all tests, the significance level for statistical analysis was set at P < 0.05. Statistical analyses were performed using STATA Version 12.0 (Stata Corporation, College Station, TX).

Result

High expression of αB-crystallin mRNA in LSCC

RT-PCR amplicons were detected by 1.5% agarose gel electrophoresis, confirming that αB-crystallin was expressed in LSCC tissues (Figure  1). Moreover, mRNA levels of αB-crystallin in LSCC tissues and tumor-adjacent tissues were determined by qPCR. Normalized to β-actin, αB-crystallin mRNA level in LSCC tissues (n = 6) and tumor-adjacent normal tissues (n = 6) was 6.808 ± 1.781 and 2.475 ± 0.757, respectively (t = 5.484, P = 0.001). mRNA level of αB-crystallin was significantly higher in LSCC than in tumor-adjacent normal tissues (Figure  2).

Figure 1.

Figure 1

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Detection of αB-crystallin mRNA expression in LSCC tissue and normal tumor-adjacent tissue. Line M: DNA marker (DL2000, TAKALA, Dalian, China); line 1: LSCC tissues; line 2: normal tumor-adjacent tissues. Shown were representative images from three independent experiments.

Figure 2.

Figure 2

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The mRNA levels of αB-crystallin determined by qPCR. The relative mRNA level of αB-crystallin was higher in LSCC than in normal tumor-adjacent tissue (p < 0.05).

αB-crystallin protein level is correlated with the clinicopathologic factors of LSCC

By immunohistochemistry analysis, we observed more positive staining cells and stronger staining in LSCC tissues than in tumor-adjacent normal tissues (Figure  3). The positive staining was localized mainly in the cytoplasm of the tumor cells and strong staining was not observed in the surrounding tumor-adjacent areas. Positive staining of αB-crystallin was detected in 64 (58.72%) of 109 LSCC samples, while only 5 cases of 28 tumor-adjacent normal tissues (17.86%) displayed high expression of αB-crystallin. There was significant difference in high expression rate of αB-crystallin between LSCC tissues and normal non-cancerous tissues (P = 0.001).

Figure 3.

Figure 3

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Expression pattern of αB-crystallin in tumor tissue and tumor-adjacent tissue of LSCC. TMA sections were analyzed by immunohistochemical staining. Brown staining indicated positive expression of αB-crystallin. A1-3: The expression pattern of αB-crystallin in moderately differentiated LSCC tissue. B1-3: The expression pattern of αB-crystallin in well-differentiated LSCC tissue. C1-2: The expression pattern of αB-crystallin in tumor-adjacent tissue with weakly positive staining of αB-crystallin. C3: Squamous epithelium of adjacent nontumorous tissue with negative staining of αB-crystallin. Original magnification: ×40 in A1, B1 and C1; ×100 in A2, B2 and C2; ×400 in A3, B3 and C3.

Correlations between various clinicopathological characteristics and αB-crystallin expression in LSCC tissues were evaluated by χ2 test (Table  1). The result showed that high expression of αB-crystallin in LSCC was significantly related to alcohol consumption (P = 0.022), tumor differentiation (P = 0.007), pTNM stage (P = 0.041) and 5-year survival (P = 0.030). However, no statistically significant correlation was found between αB-crystallin expression and gender, age, tobacco use, or lymph node metastasis.

Table 1.

Correlation of aB-crystallin expression with clinicopathological characteristics of LSCC

Groups No. aB-crystallin
 χ2 P (value)
+ %
Gender
Male
 107
 63
 58.88
 0.0638
 0.801
Female
 2
 1
 50.00
Age(years)
≤60 y
 45
 23
 51.11
 1.8283
 0.176
>60 y
 64
 41
 64.06
Tobacco use
Yes
 77
 42
 54.55
 1.8816
 0.170
No
 32
 22
 68.75
Alcohol consumption
Yes
 53
 37
 69.81
 5.2395
 0.022*
No
 56
 27
 48.21
Tumor differentiation
Well
 51
 22
 43.14
 9.9434
 0.007*
Moderate
 53
 39
 71.70
Poor
 5
 3
 80.00
pTNM stage
Stage I, II
 65
 33
 50.77
 4.1945
 0.041*
Stage III, IV
 44
 31
 70.45
Lymph node metastasis
Yes
 19
 14
 73.68
 2.1270
 0.145
No
 90
 50
 55.56
Five years’ survival
Yes
 72
 37
 51.39
 4.6972 0.030*
No 37 27 72.98
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* P < 0.05.

Survival analysis

Univariate analysis showed that the life span of LSCC patients was correlated with αB-crystallin expression (P = 0.010), pTNM stage (P < 0.001), lymph node metastasis (P < 0.001) and tumor differentiation (P = 0.022). Multivariate analysis with the Cox regression model indicated that αB-crystallin protein level may serve as an independent prognostic factor for overall survival (P = 0.013) (Table  2). Furthermore, pTNM stage (P = 0.027) and lymph node metastasis (P = 0.015) were identified as independent predictive factors for poor outcome of LSCC. Kaplan-Meier survival curves showed that patients with high αB-crystallin expression had a shorter survival time than patients with low αB-crystallin expression (Figure  4). Kaplan-Meier survival curves demonstrated that patients with high αB-crystallin expression, advanced pTNM stage of LSCC and lymph node metastasis had a significantly shorter survival time.

Table 2.

Univariate and multivariable analysis of prognostic factors in LSCC for 5-year survival

  Univariate analysis
 Multivariable analysis
HR p > |z| 95% CI HR p > |z| 95% CI
αB-crystallin expression
High versus Low
 2.508
 0.010*
 1.245-5.051
 2.498
 0.013*
 1.218-5.124
Age (years)
≤60y versus >60y
 0.613
 0.148
 0.316-1.189
  
  
  
Tobacco use
Yes versus No
 0.643
 0.203
 0.325-1.270
  
  
  
Alcohol consumption
Yes versus No
 0.903
 0.747
 0.485-1.680
  
  
  
pTNM stage
Stage I, II versus Stage III, IV
 0.291
 0.001*
 0.151-0.561
 0.426
 0.027*
 0.200-0.908
Lymph node metastasis
Yes versus No
 4.412
 0.001*
 2.225-8.748
 2.707
 0.015*
 1.215-6.034
Tumor differentiation
Well versus Moderate-Poor 0.478 0.022* 0.255-0.897 0.594 0.107 0.315-1.120
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* P < 0.05.

Figure 4.

Figure 4

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Survival curves of LSCC patients based on various independent factors.A: Overall survival rate in patients with positive expression of αB-crystallin (red line, αB-crystallin = 1) was significantly lower than that in patients with negative αB-crystallin expression (green line, αB-crystallin = 0). B: Overall survival rate in patients with stage III-IV of LSCC (red line, stage III-IV = 0) was significantly lower than that in patients with stage I-II of LSCC (green line, stage I-II = 1). C: Overall survival rate in patients with lymph node metastasis (red line, LN metastasis = 1) was significantly lower than that in patients without lymph node metastasis (green line, LN metastasis = 0).

Discussion

Several state-of-the-art treatment strategies have been developed for LSCC, including molecular targeted therapy [18], gene therapy [19] and immunotherapy [20]. However, no treatment could achieve satisfactory therapeutic outcome and the survival rate of LSCC has not been improved significantly [21]. Recent studies suggest several molecular markers of LSCC [22-24]. Further identification of prognostic markers for LSCC will be important for the prevention and therapy of LSCC.

αB-crystallin has been shown to be overexpressed in numerous kinds of tumors, including gliomas, prostate cancer, oral squamous cell carcinomas, renal cell carcinomas, and head and neck cancer [25]. Recently, an oncogenic role of αB-crystallin has been proposed for breast cancer [26]. The neoplastic changes and invasive phenotypes of breast cells and the anti-apopototic activities of αB-crystallin were inhibited by the phosphorylation of αB-crystallin [27,28]. Furthermore, αB-crystallin could promote tumor angiogenesis by modulating VEGF [13,14]. These studies demonstrate that αB-crystallin plays crucial role in tumor progression.

In the present study, the mRNA and protein levels of αB-crystallin in LSCC and tumor-adjacent normal tissues were detected by qPCR and immunohistochemistry. Both analyses showed that αB-crystallin was highly expressed in LSCC compared to tumor-adjacent normal tissues. These results agree with previous report which showed that αB-crystallin was overexpressed in hepatocellular carcinoma cells compared with non-tumour cells [11]. Moreover, we found that the high expression of αB-crystallin in LSCC was related to alcohol consumption, tumor differentiation, pTNM stage and 5-year survival.

Univariate analysis showed that not only αB-crystallin expression, but also the pTNM stage, lymph node metastasis and tumor differentiation were correlated with life span of LSCC patients. Multivariate analysis revealed that strong expression of αB-crystallin could be considered as an independent factor for poor prognosis of LSCC patients, as well as pTNM stage and lymph node metastasis.

Interestingly, several studies suggest that αB-crystallin acts as a tumor suppressor gene in certain types of cancer [29-31]. In addition, αB-crystallin staining was reported to be reduced in head and neck squamous cell carcinoma and αB-crystallin was not proposed as a prognostic marker [32,33]. Our present data are inconsistent with these studies. These conflicting results may be due to the differences in the pathological samples, the antibodies used, the experimental methods or evaluation system.

In conclusion, to the best of our knowledge, this is the first study to report that high αB-crystallin expression is correlated with aggressive malignant phenotype of LSCC. Our data indicate that αB-crystallin may serve as a novel prognostic marker for LSCC. Further studies are needed to confirm the prognostic and therapeutic value of αB-crystallin for LSCC.

Conclusions

Taken together, the results of this study suggest that αB-crystallin expression is correlated with malignant phenotypes of LSCC and it may serve as a novel prognostic factor for LSCC.

Competing interests

The authors declared that they have no competing interest.

Authors’ contributions

YM and DWZ design the study; HL, YL and QDL carried out the RT-PCR and qPCR analysis; LX, JM and QC peformed the immunohistochemistry; YM drafted the manuscript. All authors read and approved the final manuscript.

Contributor Information

Yuan Mao, Email: ymaoent@yahoo.com.

Da-Wei Zhang, Email: chinarenzdw@yahoo.com.cn.

Hong Lin, Email: linhong712003@yahoo.com.cn.

Lin Xiong, Email: nypiag@sohu.com.

Ying Liu, Email: future616@126.com.

Qing-Dong Li, Email: liqingdong2012@126.com.

Jun Ma, Email: 936965157@qq.com.

Qing Cao, Email: ufo-43@163.com.

Ren-Jie Chen, Email: renjiechenent@yahoo.com.cn.

Jin Zhu, Email: zjsimmons@yahoo.com.cn.

Zhen-Qing Feng, Email: fengzhenqing@njmu.edu.cn.

Acknowledgments

This work is supported by the grants from General Program of Jiangsu Province Official Hospital (No. L201109) and Youth Funds of Second Affiliated Hospital of Nanjing Medical University (No. QN201004).

References

  1. Wu H, Xu H, Zhang S, Wang X, Zhu H, Zhang H, Zhu J, Huang J. Potential therapeutic target and independent prognostic marker of TROP2 in laryngeal squamous cell carcinoma. Head Neck. 2012. doi:10.1002/hed.23138. [DOI] [PubMed]
  2. Jemal A, Siegel R, Ward E, Hao Y, Xu J, Thun MJ. Cancer statistics, 2009. CA Cancer J Clin. 2009;59(4):225–249. doi: 10.3322/caac.20006. [DOI] [PubMed] [Google Scholar]
  3. Hoffman HT, Porter K, Karnell LH, Cooper JS, Weber RS, Langer CJ, Ang KK, Gay G, Stewart A, Robinson RA. Laryngeal cancer in the United States: changes in demographics, patterns of care, and survival. Laryngoscope. 2006;116(9 Pt 2 Suppl 111):1–13. doi: 10.1097/01.mlg.0000236095.97947.26. [DOI] [PubMed] [Google Scholar]
  4. Boyle P, Ferlay J. Cancer incidence and mortality in Europe. Ann Oncol. 2005;16(3):481–488. doi: 10.1093/annonc/mdi098. [DOI] [PubMed] [Google Scholar]
  5. Chin D, Boyle GM, Williams RM, Ferguson K, Pandeya N, Pedley J, Campbell CM, Theile DR, Parsons PG, Coman WB. Alpha B-crystallin, a new independent marker for poor prognosis in head and neck cancer. Laryngoscope. 2005;115(7):1239–1242. doi: 10.1097/01.MLG.0000164715.86240.55. [DOI] [PubMed] [Google Scholar]
  6. Moyano JV, Evans JR, Chen F, Lu M, Werner ME, Yehiely F, Diaz LK, Turbin D, Karaca G, Wiley E, Nielsen TO, Perou CM, Cryns VL. AlphaB-crystallin is a novel oncoprotein that predicts poor clinical outcome in breast cancer. J Clin Invest. 2006;116(1):261–270. doi: 10.1172/JCI25888. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Kamradt MC, Lu M, Werner ME, Kwan T, Chen F, Strohecker A, Oshita S, Wilkinson JC, Yu C, Oliver PG, Duckett CS, Buchsbaum DJ, LoBuglio AF, Jordan VC, Cryns VL. The small heat shock protein alpha B-crystallin is a novel inhibitor of TRAIL-induced apoptosis that suppresses the activation of caspase-3. J Biol Chem. 2005;280(12):11059–11066. doi: 10.1074/jbc.M413382200. [DOI] [PubMed] [Google Scholar]
  8. Adhikari AS, Singh BN, Rao KS, Rao CM. αB-crystallin, a small heat shock protein, modulates NF-κB activity in a phosphorylation-dependent manner and protects muscle myoblasts from TNF-α induced cytotoxicity. Biochim Biophys Acta. 2011;1813(8):1532–1542. doi: 10.1016/j.bbamcr.2011.04.009. [DOI] [PubMed] [Google Scholar]
  9. Mao YW, Liu JP, Xiang H, Li DW. Human alphaA- and alphaBcrystallins bind to Bax and Bcl-X(S) to sequester their translocation during staurosporine-induced apoptosis. Cell Death Differ. 2004;11(5):512–526. doi: 10.1038/sj.cdd.4401384. [DOI] [PubMed] [Google Scholar]
  10. Chan SK, Lui PC, Tan PH, Yamaguchi R, Moriya T, Yu AM, Shao MM, Hliang T, Wong SI, Tse GM. Increased alpha-B-crystallin expression in mammary metaplastic carcinomas. Histopathology. 2011;59(2):247–255. doi: 10.1111/j.1365-2559.2011.03882.x. [DOI] [PubMed] [Google Scholar]
  11. Tang Q, Liu YF, Zhu XJ, Li YH, Zhu J, Zhang JP, Feng ZQ, Guan XH. Expression and prognostic significance of the αB-crystallin gene in human hepatocellular carcinoma. Hum Pathol. 2009;40(3):300–305. doi: 10.1016/j.humpath.2008.09.002. [DOI] [PubMed] [Google Scholar]
  12. Stegh AH, Kesari S, Mahoney JE, Jenq HT, Forloney KL, Protopopov A, Louis DN, Chin L, DePinho RA. Bcl2L12-mediated inhibition of effector caspase-3 and caspase-7 via distinct mechanisms in glioblastoma. Proc Natl Acad Sci USA. 2008;105(31):10703–10708. doi: 10.1073/pnas.0712034105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Dimberg A, Rylova S, Dieterich LC, Olsson AK, Schiller P, Wikner C, Bohman S, Botling J, Lukinius A, Wawrousek EF, Claesson-Welsh L. alphaB-crystallin promotes tumor angiogenesis by increasing vascular survival during tube morphogenesis. Blood. 2008;111(4):2015–2023. doi: 10.1182/blood-2007-04-087841. [DOI] [PubMed] [Google Scholar]
  14. Kase S, He S, Sonoda S, Kitamura M, Spee C, Wawrousek E, Ryan SJ, Kannan R, Hinton DR. alphaB-crystallin regulation of angiogenesis by modulation of VEGF. Blood. 2010;115(16):3398–3406. doi: 10.1182/blood-2009-01-197095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Thompson L. World Health Organization classification of tumours: pathology and genetics of head and neck tumours. Ear Nose Throat J. 2006;85(2):74. [PubMed] [Google Scholar]
  16. Friedrich M, Villena-Heinsen C, Reitnauer K, Schmidt W, Tilgen W, Reichrath J. Malignancies of the uterine corpus and immunoreactivity score of the DNA “mismatch-repair”enzyme human Mut-S-homologon-2. J Histochem Cytochem. 1999;47(1):113–118. doi: 10.1177/002215549904700112. [DOI] [PubMed] [Google Scholar]
  17. Mao Y, Zhang DW, Wen J, Cao Q, Chen RJ, Zhu J, Feng ZQ. A novel LMP1 antibody synergizes with Mitomycin C to inhibit Nasopharyngeal Carcinoma growth in vivo through inducing apoptosis and downregulating vascular endothelial growth factor. Int J Mol Sci. 2012;13(2):2208–2218. doi: 10.3390/ijms13022208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Luo XM, Zhou SH, Fan J. Glucose transporter-1 as a new therapeutic target in laryngeal carcinoma. J Int Med Res. 2010;38(6):1885–1892. doi: 10.1177/147323001003800601. [DOI] [PubMed] [Google Scholar]
  19. Chen J, Yang B, Zhang S, Ling Y, Ye J, Jia Z, Cao J. Antitumor potential of SLPI promoter controlled recombinant caspase-3 expression in laryngeal carcinoma. Cancer Gene Ther. 2012;19(5):328–335. doi: 10.1038/cgt.2012.5. [DOI] [PubMed] [Google Scholar]
  20. Liang W, Wang XF. In vitro induction of specific anti-tumoral immunity against laryngeal carcinoma by using human interleukin-12 gene-transfected dendritic cells. Chin Med J (Engl) 2011;124(9):1357–1361. [PubMed] [Google Scholar]
  21. de Souza DL B, Jerez Roig J, Bernal MM. Laryngeal cancer survival in Zaragoza (Spain): a population-based study. Clin Transl Oncol. 2012;14(3):221–224. doi: 10.1007/s12094-012-0787-1. [DOI] [PubMed] [Google Scholar]
  22. Liu Y, Dong XL, Tian C, Liu HG. Human telomerase RNA component (hTERC) gene amplification detected by FISH in precancerous lesions and carcinoma of the larynx. Diagn Pathol. 2012;7:34. doi: 10.1186/1746-1596-7-34. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Shi Y, Gong HL, Zhou L, Tian J, Wang Y. CD24: a novel cancer biomarker in laryngeal squamous cell carcinoma. ORL J Otorhinolaryngol Relat Spec. 2012;74(2):78–85. doi: 10.1159/000335584. [DOI] [PubMed] [Google Scholar]
  24. Liu J, Lei DP, Jin T, Zhao XN, Li G, Pan XL. Altered expression of miR-21 and PTEN in human laryngeal and hypopharyngeal squamous cell carcinomas. Asian Pac J Cancer Prev. 2011;12(10):2653–2657. [PubMed] [Google Scholar]
  25. Arrigo AP, Simon S, Gibert B, Kretz-Remy C, Nivon M, Czekalla A, Guillet D, Moulin M, Diaz-Latoud C, Vicart P. Hsp27 (HspB1) and alphaB-crystallin (HspB5) as therapeutic targets. FEBS Lett. 2007;581(19):3665–3674. doi: 10.1016/j.febslet.2007.04.033. [DOI] [PubMed] [Google Scholar]
  26. Gruvberger-Saal SK, Parsons R. Is the small heat shock protein alphaB-crystallin an oncogene? J Clin Invest. 2006;116(1):30–32. doi: 10.1172/JCI27462. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Chelouche-Lev D, Kluger HM, Berger AJ, Rimm DL, Price JE. alphaB-crystallin as a marker of lymphnode involvement in breast carcinoma. Cancer. 2004;100(12):2543–2548. doi: 10.1002/cncr.20304. [DOI] [PubMed] [Google Scholar]
  28. Jeong WJ, Rho JH, Yoon YG, Yoo SH, Jeong NY, Ryu WY, Ahn HB, Park WC, Rho SH, Yoon HS, Choi YH, Yoo YH. Cytoplasmic and nuclear anti-apoptotic roles of αB-Crystallin in retinal pigment epithelial cells. PLoS One. 2012;7(9):e45754. doi: 10.1371/journal.pone.0045754. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Huang Z, Cheng Y, Chiu PM, Cheung FM, Nicholls JM, Kwong DL, Lee AW, Zabarovsky ER, Stanbridge EJ, Lung HL, Lung ML. Tumor suppressor Alpha B-crystallin (CRYAB) associates with the cadherin/catenin adherens junction and impairs NPC progression-associated properties. Oncogene. 2012;31(32):3709–3720. doi: 10.1038/onc.2011.529. [DOI] [PubMed] [Google Scholar]
  30. Barbash O, Zamfirova P, Lin DI, Chen X, Yang K, Nakagawa H, Lu F, Rustgi AK, Diehl JA. Mutations in Fbx4 inhibit dimerization of the SCF(Fbx4) ligase and contribute to cyclin D1 overexpression in human cancer. Cancer Cell. 2008;14(1):68–78. doi: 10.1016/j.ccr.2008.05.017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Stronach EA, Sellar GC, Blenkiron C, Rabiasz GJ, Taylor KJ, Miller EP, Massie CE, Al-Nafussi A, Smyth JF, Porteous DJ, Gabra H. Identification of clinically relevant genes on chromosome 11 in a functional model of ovarian cancer tumor suppression. Cancer Res. 2003;63(24):8648–8655. [PubMed] [Google Scholar]
  32. Solares CA, Boyle GM, Brown I, Parsons PG, Panizza B. Reduced alphaB-crystallin staining in perineural invasion of head and neck cutaneous squamous cell carcinoma. Otolaryngol Head Neck Surg. 2010;142(3 Suppl 1):S15–S19. doi: 10.1016/j.otohns.2009.12.001. [DOI] [PubMed] [Google Scholar]
  33. Boslooper K, King-Yin Lam A, Gao J, Weinstein S, Johnson N. The clinicopathological roles of alpha-B-crystallin and p53 expression in patients with head and neck squamous cell carcinoma. Pathology. 2008;40(5):500–504. doi: 10.1080/00313020802198010. [DOI] [PubMed] [Google Scholar]

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