Evidence map›Paper›PMID 31208298›Full record

ArticleAutophagy2020

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

Sulin Zhang, Zhiwen Yang, Weilian Bao, Lixin Liu, Yan You, Xu Wang, Liming Shao, Wei Fu, Xinhui Kou, Weixing Shen and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.2field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. The molecular and functional interplay between the osteopetrosis-associated proteins SNX10, OSTM1, and CLC-7 during mouse osteoclastogenesis.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2026
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  12. Unveiling SNX10: a key player in bladder cancer progression.Translational andrology and urology · 2025
    Article
  13. Inhibiting SNX10 induces autophagy to suppress invasion and EMT and inhibits the PI3K/AKT pathway in cervical cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 1 country.

Sulin ZhangDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Zhiwen YangDepartment of Pharmacy, Songjiang Hospital Affiliated Shanghai First People's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Weilian BaoDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Lixin LiuDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Yan YouDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Xu WangDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Liming ShaoDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Wei FuDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Xinhui KouDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Weixing ShenThe Translational Medicine Research Center, Nanjing University of Traditional Chinese Medicine, Nanjing, China.
Congmin YuanDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Bin HuDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Wenzhen DangDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Kutty Selva NandakumarSchool of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.ORCID 0000-0001-7790-8197
Hualiang JiangDrug Discovery and Design Center, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Mingyue ZhengDrug Discovery and Design Center, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Xiaoyan ShenDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Fudan University · CNChinese Academy of Sciences · CNShanghai Jiao Tong University · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AnimalsAutophagyCell MovementColorectal NeoplasmsDown-RegulationHumansLysosomesMiceMicrotubule-Associated ProteinsProto-Oncogene MasSorting NexinsUp-RegulationMAS1 protein, humanMicrotubule-Associated ProteinsProto-Oncogene MasSNX10 protein, humanSNX10 protein, mouseSorting NexinsColorectal cancermacroautophagySNX10SRCtumor growth

Identifiers

PMID31208298
PMCPMC7138201
OpenAlexW2950030327

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.