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. 2015 Dec 30;8(1):4. doi: 10.3390/cancers8010004

Table 1.

The suppression effects of transformed phenotypes following introduction of normal human chromosomes into various tumor cell types.

Transferred Chromosome Cell Lines Type Mapping Region Reference
1 2 3 4 5
1 HT1080 (fibrosarcoma) + + [30]
TE85(osteosarcoma) + [44]
143 B (TK-Ki-Ras-transformed TE85) + [44]
CMV-Mj-HEL-1 (CMV-transfermed lung fibroblasts) + [44]
10W-2 (immortal Syrian hamster fibroblasts) + [51]
Isikawa (uterine endomerial carcinoma) + *
HHUA (uterine endometrial carcinoma) + + [45]
2 SiHa (cervical cancer) + 2q37 [31,32]
3 RCC23 (renal cell carcinoma) + + 3p21.3 [40,46,54]
KC12 (renal cell carcinoma) + + 3p14.2-p21.1 [33]
HSC3 (oral squamous cell carcinoma) + + + 3p21.2-p21.3 or 3p25 [41,55]
TS1 (lung adenocarcinoma) + *
4 HeLa (cevical cancer) + [47]
J82 (baladder cancer) + [47]
T98G (glioblastoma) + [47]
5 A2058 (melanoma) + + [26,39]
6 HALneo (immortal fibroblasts) + [48]
LCS-AF.1-3 (immortal fibroblasts) + 6p23-p24 [56]
39neo (immortal fibroblasts) + [48]
SV/HF (SV40-tranformed fibroblasts) + [48]
HPV-16 (HPV-immortalized keratinocyte) + [53]
7 KMST-6 (immortal fibroblasts) + [49]
SUSM-1 (immortal fibroblasts) + [49]
CC1 (choriocarcinoma) + *
R-3327 (rat prostatic cancer cells) + 7q21-22, 7q31.2-32 [57]
MeT5A (mesothelial cells) + + [52]
8 R-3327 (rat prostatic cancer cells) + 8p21-q12 [57]
10 Li7HM (hepatocellular carcinoma) + + 10p15.1 [35]
R-3327 (rat prostatic cancer cells) + 10q11-22 [57]
11 HeLa (cevical cancer) + [58]
G401 (wilm’s tumor) + + [59]
SiHa (cervical cancer) + [29]
A204 (rhadboyomyosarcoma) + [29]
HHUA (uterine endometrial carcinoma) + [29]
HT1080 (fibrosarcoma) + [30]
RD (rhabdomyosarcoma) + [50]
H15 (bladder cancer) + *
R-3327 (rat prostatic cancer cells) + 11p13-11.2 [57]
13 R-3327 (rat prostatic cancer cells) + [60]
17 R-3327 (rat prostatic cancer cells) + 12p11-q13, 12q24-ter [57]
18 HHUA (uterine endometrial carcinoma) + + [45]
X HocB (ovarian carcinoma) + *
ELCO (breast carcinoma) + *

Type 1: Induced senescence; Type 2: Suppression of in vitro transformed; Type 3: Suppression of tumorigenicity; Type 4: Suppression of telomerase activity; *: Unpublished data by the authors; +: Effective.