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SNX10 (sorting nexin 10) inhibits colorectal cancer initiation and progression by controlling autophagic degradation of SRC

Zhang, Sulin (författare)
School of Pharmacy, Fudan University, Shanghai, China; Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China
Yang, Zhiwen (författare)
Shanghai Jiao Tong University, Shanghai, China
Bao, Weilian (författare)
School of Pharmacy, Fudan University, Shanghai, China
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Liu, Lixin (författare)
School of Pharmacy, Fudan University, Shanghai, China
You, Yan (författare)
School of Pharmacy, Fudan University, Shanghai, China
Wang, Xu (författare)
School of Pharmacy, Fudan University, Shanghai, China
Shao, Liming (författare)
School of Pharmacy, Fudan University, Shanghai, China
Fu, Wei (författare)
School of Pharmacy, Fudan University, Shanghai, China
Kou, Xinhui (författare)
School of Pharmacy, Fudan University, Shanghai, China
Shen, Weixing (författare)
Nanjing University of Traditional Chinese Medicine, Nanjing, China
Yuan, Congmin (författare)
School of Pharmacy, Fudan University, Shanghai, China
Hu, Bin (författare)
School of Pharmacy, Fudan University, Shanghai, China
Dang, Wenzhen (författare)
School of Pharmacy, Fudan University, Shanghai, China
Nandakumar, Kutty Selva, 1965- (författare)
Southern Medical University, Guangzhou, China
Jiang, Hualiang (författare)
Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China
Zheng, Mingyue (författare)
Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China
Shen, Xiaoyan (författare)
School of Pharmacy, Fudan University, Shanghai, China
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 (creator_code:org_t)
2019-07-04
2020
Engelska.
Ingår i: Autophagy. - Philadelphia : Taylor & Francis. - 1554-8627 .- 1554-8635. ; 16:4, s. 735-749
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The non-receptor tyrosine kinase SRC is a key mediator of cellular protumorigenic signals. SRC is aberrantly over-expressed and activated in more than 80% of colorectal cancer (CRC) patients, therefore regulation of its stability and activity is essential. Here, we report a significant down regulation of SNX10 (sorting nexin 10) in human CRC tissues, which is closely related to tumor differentiation, TNM stage, lymph node metastasis and survival period. SNX10 deficiency in normal and neoplastic colorectal epithelial cells promotes initiation and progression of CRC in mice. SNX10 controls SRC levels by mediating autophagosome-lysosome fusion and SRC recruitment for autophagic degradation. These mechanisms ensure proper controlling of the activities of SRC-STAT3 and SRC-CTNNB1 signaling pathways by up-regulating SNX10 expression under stress conditions. These findings suggest that SNX10 acts as a tumor suppressor in CRC and it could be a potential therapeutic target for future development.Abbreviations: ACTB: actin beta; ATG5: autophagy related 5; ATG12: autophagy related 12; CQ: chloroquine; CRC: colorectal cancer; CTNNB1: catenin beta 1; EBSS: Earle's balanced salt solution; KO: knockout; LAMP1: lysosomal associated membrane protein 1; LAMP2: lysosomal associated membrane protein 2; MAP1LC3: microtubule associated protein 1 light chain 3; MKI67: marker of proliferation Ki-67; mRNA: messenger RNA; PX: phox homology; RT-qPCR: real time quantitative polymerase chain reaction; siRNA: small interfering RNA; SNX10: sorting nexin 10; SQSTM1: sequestosome 1; SRC: SRC proto-oncogene, non-receptor tyrosine kinase; STAT3: signal transducer and activator of transcription 3; WT: wild type. © 2019 Informa UK Limited, trading as Taylor & Francis Group

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Nyckelord

Colorectal cancer
SNX10
SRC
macroautophagy
tumor growth

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