首页> 外文期刊>International journal of biological sciences >Differences in Apoptosis and Cell Cycle Distribution between Human Melanoma Cell Lines UACC903 and UACC903(+6), before and after UV Irradiation
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Differences in Apoptosis and Cell Cycle Distribution between Human Melanoma Cell Lines UACC903 and UACC903(+6), before and after UV Irradiation

机译:紫外线照射前后人黑素瘤细胞株UACC903和UACC903(+6)的凋亡和细胞周期分布差异

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Introduction of human chromosome 6 into malignant melanoma cell line UACC903 resulted in generation of the chromosome 6-mediated suppressed cell subline UACC903(+6) that displays attenuated growth rate, anchorage-dependency, and reduced tumorigenicity. We have showed that overexpression of a chromosome 6-encoded tumor suppressor gene led to partial suppression to UACC903 cell growth. We now describe the differences in apoptosis and cell cycle between UACC903 and UACC903(+6) before and after UV irradiation. MTT assay revealed 86.92±8.24% of UACC903 cells viable, significantly (p<0.01) higher than 48.76±5.31% of UACC903(+6), at 24 hr after 254-nm UV irradiation (40 J/M2). Before UV treatment, flow cytometry analysis revealed 6.06±0.20% apoptosis in UACC903, significantly (p=0.01) lower than 6.67±0.15% in UACC903(+6). The G0/G1, S and G2/M phase cells of UACC903 were, respectively, 54.10±0.59%, 22.31±0.50% and 16.85±0.25%, all significantly (p<0.01) different from the corresponding percentages (58.82±0.35%, 20.48±0.05%, and 13.17±0.45%) of UACC903(+6). After the UV treatment, UACC903 cells in apoptosis, G0/G1, S, and G2/M became 12.59±0.17%, 38.90±0.67%, 19.74±0.70%, and 27.01±0.66%, respectively, while UACC903(+6) cells were 24.16±0.48%, 37.97±0.62%, 19.20±0.52%, and 15.69±0.14%. TUNEL assay revealed 2.31±0.62% apoptosis in UACC903, significantly (p<0.01) lower than 9.60±1.14% of UACC903(+6), and a linear and exponential increase of apoptosis, respectively, in response to the UV treatment. These results indicate that UACC903(+6) cells have a greater tendency to undergo apoptosis and are thus much more sensitive to UV irradiation. Our findings further suggest a novel mechanism for chromosome 6-mediated suppression of tumorigenesis and metastasis, i.e., through increased cell death.
机译:将人类6号染色体引入恶性黑色素瘤细胞系UACC903导致了6号染色体介导的抑制细胞亚系UACC903(+6)的产生,该亚细胞显示出生长速率降低,锚定依赖性和致瘤性降低。我们已经表明,染色体6编码的肿瘤抑制基因的过表达导致对UACC903细胞生长的部分抑制。我们现在描述紫外线照射前后UACC903和UACC903(+6)之间的凋亡和细胞周期的差异。 MTT分析显示,在254 nm UV照射(40 J / M2)后24小时,UACC903细胞的存活率为86.92±8.24%,显着(p <0.01)高于UACC903(+6)的48.76±5.31%。在紫外线处理之前,流式细胞仪分析显示UACC903中的凋亡为6.06±0.20%,显着(p = 0.01)低于UACC903中的6.67±0.15%(+ 6)。 UACC903的G0 / G1,S和G2 / M期细胞分别为54.10±0.59%,22.31±0.50%和16.85±0.25%,均与相应百分比(58.82±0.35%)显着不同(p <0.01) ,UACC903(+6)的20.48±0.05%和13.17±0.45%)。紫外线处理后,UACC903细胞凋亡,G0 / G1,S和G2 / M分别为12.59±0.17%,38.90±0.67%,19.74±0.70%和27.01±0.66%,而UACC903(+6)细胞为24.16±0.48%,37.97±0.62%,19.20±0.52%和15.69±0.14%。 TUNEL分析显示,UACC903中的细胞凋亡为2.31±0.62%,显着(p <0.01)低于UACC903(9.6)的9.60±1.14%(+ 6),并且响应于紫外线处理,凋亡呈线性和指数增加。这些结果表明,UACC903(+6)细胞具有更大的凋亡倾向,因此对紫外线照射更为敏感。我们的发现进一步提出了染色体6介导的肿瘤发生和转移抑制的新机制,即通过增加的细胞死亡。

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