Department of Gastroenterological, Breast and Endocrine Surgery, Graduate School of Medicine, Yamaguchi University, Ube, Japan.
Laboratory of Drug Discovery and Pharmacology, Faculty of Veterinary Medicine, Okayama University of Science, Imabari, Japan.
Cancer Sci. 2024 Sep;115(9):3067-3078. doi: 10.1111/cas.16271. Epub 2024 Jul 16.
Colorectal cancer (CRC) remains a significant global health concern, demanding a more profound comprehension of its molecular foundations for the development of improved therapeutic strategies. This study aimed to elucidate the role of protein phosphatase 6 (PP6), a member of the type 2A protein phosphatase family, in CRC. Protein phosphatase 6 functions as a heterotrimer with a catalytic subunit (PP6c), regulatory subunits (PP6Rs; PP6R1, PP6R2, and PP6R3), and scaffold subunits (ANKRD28, ANKRD44, and ANKRD52). Elevated PP6c expression has been identified in CRC tissues compared to normal mucosa, aligning with its potential involvement in CRC pathogenesis. PP6c knockdown resulted in decreased colony-forming ability and in vivo proliferation of various CRC cell lines. Transcriptome analysis revealed that PP6c knockdown resulted in altered expression of genes associated with cancer stemness. Notably, the PP6c-PP6R3 complex is a key player in regulating cancer stem cell (CSC) markers. Additionally, increased PP6c expression was observed in CSC-like cells induced by sphere formation, implicating the role of PP6c in CSC maintenance. This study highlights the role of PP6c in CRC and suggests that it is a potential therapeutic target disrupting a pathway critical for CRC progression and stem cell maintenance.
结直肠癌(CRC)仍然是一个重大的全球健康问题,需要更深入地了解其分子基础,以制定改进的治疗策略。本研究旨在阐明蛋白磷酸酶 6(PP6)在 CRC 中的作用。PP6 作为一种由催化亚基(PP6c)、调节亚基(PP6R;PP6R1、PP6R2 和 PP6R3)和支架亚基(ANKRD28、ANKRD44 和 ANKRD52)组成的异三聚体发挥作用。与正常黏膜相比,CRC 组织中 PP6c 的表达升高,这与其在 CRC 发病机制中的潜在作用一致。PP6c 敲低导致各种 CRC 细胞系的集落形成能力和体内增殖能力下降。转录组分析显示,PP6c 敲低导致与癌症干性相关的基因表达发生改变。值得注意的是,PP6c-PP6R3 复合物是调节癌症干细胞(CSC)标志物的关键因素。此外,在球体形成诱导的 CSC 样细胞中观察到 PP6c 表达增加,表明 PP6c 在 CSC 维持中的作用。本研究强调了 PP6c 在 CRC 中的作用,并表明它是一种潜在的治疗靶点,可破坏 CRC 进展和干细胞维持的关键途径。