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Protein phosphatase 6 promotes stemness of colorectal cancer cells.
Fujiwara, Nobuyuki; Tsunedomi, Ryouichi; Kimura, Yuta; Nakajima, Masao; Tomochika, Shinobu; Enjoji, Shuhei; Ohama, Takashi; Sato, Koichi; Nagano, Hiroaki.
Affiliation
  • Fujiwara N; Department of Gastroenterological, Breast and Endocrine Surgery, Graduate School of Medicine, Yamaguchi University, Ube, Japan.
  • Tsunedomi R; Laboratory of Drug Discovery and Pharmacology, Faculty of Veterinary Medicine, Okayama University of Science, Imabari, Japan.
  • Kimura Y; Department of Gastroenterological, Breast and Endocrine Surgery, Graduate School of Medicine, Yamaguchi University, Ube, Japan.
  • Nakajima M; Research Institute for Cell Design Medical Science, Yamaguchi University, Ube, Japan.
  • Tomochika S; Department of Gastroenterological, Breast and Endocrine Surgery, Graduate School of Medicine, Yamaguchi University, Ube, Japan.
  • Enjoji S; Department of Gastroenterological, Breast and Endocrine Surgery, Graduate School of Medicine, Yamaguchi University, Ube, Japan.
  • Ohama T; Department of Gastroenterological, Breast and Endocrine Surgery, Graduate School of Medicine, Yamaguchi University, Ube, Japan.
  • Sato K; Laboratory of Veterinary Pharmacology, Faculty of Veterinary Medicine, Yamaguchi University, Yamaguchi, Japan.
  • Nagano H; Research Institute for Cell Design Medical Science, Yamaguchi University, Ube, Japan.
Cancer Sci ; 2024 Jul 16.
Article in En | MEDLINE | ID: mdl-39014521
ABSTRACT
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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cancer Sci Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cancer Sci Year: 2024 Document type: Article Affiliation country: