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全面分析小鼠癌/睾丸抗原在癌细胞中的功能及 TEKT5 在癌细胞和睾丸生殖细胞中的作用。

Comprehensive Analysis of Mouse Cancer/Testis Antigen Functions in Cancer Cells and Roles of TEKT5 in Cancer Cells and Testicular Germ Cells.

机构信息

Cell Resource Center for Biomedical Research, Institute of Development, Aging and Cancer, Tohoku University, Sendai, Miyagi, Japan.

Graduate School of Life Sciences, Tohoku University, Sendai, Miyagi, Japan.

出版信息

Mol Cell Biol. 2019 Aug 12;39(17). doi: 10.1128/MCB.00154-19. Print 2019 Sep 1.

Abstract

The cancer/testis antigen (CTA) genes were identified as human genes preferentially expressed in cancer cells and testis, but the contribution of CTAs to cancer and male germ cell development is unclear. In this study, we comprehensively examined mouse CTA functions and found that the majority of CTAs are involved in growth and/or survival of cancer cells. We focused on one mouse CTA gene, , for its detailed functional analysis. knockdown (KD) in ovarian cancer cells caused G arrest and apoptosis, and p27 was concomitantly upregulated. KD also resulted in decreased levels of acetylated α-tubulin and subsequent fragmentation of β-III-tubulin, upregulation of HDAC6 that deacetylates α-tubulin, and nuclear accumulation of SMAD3 that induces p27 expression. Because depolymerization of tubulin is known to cause translocation of SMAD3 to the nucleus, these results together suggested that TEKT5 negatively regulates expression and consequently maintains cell cycle via stabilization of tubulin. We also found that the number of spermatids was significantly decreased and acetylated α-tubulin levels were decreased by KD of in testis. Because acetylated α-tubulin is required for sperm morphogenesis, these results suggest that TEKT5 is necessary for spermiogenesis via maintenance of acetylated α-tubulin levels.

摘要

癌症/睾丸抗原(CTA)基因被鉴定为在癌细胞和睾丸中优先表达的人类基因,但 CTA 对癌症和男性生殖细胞发育的贡献尚不清楚。在这项研究中,我们全面研究了小鼠 CTA 的功能,发现大多数 CTA 参与癌细胞的生长和/或存活。我们专注于一个小鼠 CTA 基因,TEKT5,进行其详细的功能分析。TEKT5 在卵巢癌细胞中的敲低(KD)导致 G1 期阻滞和细胞凋亡,同时 p27 上调。TEKT5 敲低还导致乙酰化α-微管蛋白水平降低,随后β-III-微管蛋白片段化,HDAC6 上调(其去乙酰化α-微管蛋白),以及 SMAD3 核内积累(诱导 p27 表达)。因为众所周知微管蛋白的解聚会导致 SMAD3 向核内易位,这些结果共同表明 TEKT5 通过稳定微管蛋白负调控表达,并因此维持细胞周期。我们还发现,TEKT5 在睾丸中的敲低导致精子细胞数量显著减少,乙酰化α-微管蛋白水平降低。因为乙酰化α-微管蛋白是精子形态发生所必需的,这些结果表明 TEKT5 通过维持乙酰化α-微管蛋白水平对精子发生是必要的。

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