Evidence map›Paper›PMID 37151875›Full record

ArticleInternational journal of biological sciences2023

CTSG Suppresses Colorectal Cancer Progression through Negative Regulation of Akt/mTOR/Bcl2 Signaling Pathway.

Shixin Chan, Xu Wang, Zhenglin Wang, Youwen Du, Xiaomin Zuo, Jiajie Chen, Rui Sun, Qing Zhang, Li Lin, Yang Yang and 4 more

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 33 citations in OpenAlex.

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  4. It's a Trap!-Potential of Cathepsins in NET Formation.International journal of molecular sciences · 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

14 authors at 4 institutions in 1 country.

Shixin ChanDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei 230032, Anhui, China.
Xu WangDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei 230032, Anhui, China.
Zhenglin WangDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei 230032, Anhui, China.
Youwen DuSchool of Life Sciences, Anhui Medical University, Hefei 230022, Anhui, China.
Xiaomin ZuoDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei 230032, Anhui, China.
Jiajie ChenDepartment of Dermatology, First Affiliated Hospital of Anhui Medical University, Hefei 230022, Anhui, China.
Rui SunDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei 230032, Anhui, China.
Qing ZhangDepartment of Biochemistry and Molecular Biology, Metabolic Disease Research Center, School of Basic Medicine, Anhui Medical University, Hefei 230032, Anhui, China.
Li LinDepartment of Biochemistry and Molecular Biology, Metabolic Disease Research Center, School of Basic Medicine, Anhui Medical University, Hefei 230032, Anhui, China.
Yang YangDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei 230032, Anhui, China.
Zhen YuDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei 230032, Anhui, China.
Hu ZhaoDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei 230032, Anhui, China.
Huabing ZhangDepartment of Biochemistry and Molecular Biology, Metabolic Disease Research Center, School of Basic Medicine, Anhui Medical University, Hefei 230032, Anhui, China.
Wei ChenDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei 230032, Anhui, China.
Anhui Medical University · CNFirst Affiliated Hospital of Anhui Medical University · CNAnhui Provincial Hospital · CNChuzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is the most common gastrointestinal tumor worldwide, which is a severe malignant disease that threatens mankind. Cathepsin G (CTSG) has been reported to be associated with tumorigenesis, whereas its role in CRC is still unclear. This investigation aims to determine the function of CTSG in CRC. Our results indicated that CTSG was inhibited in CRC tissues, and patients with CTSG low expression have poor overall survival. Functional experiments revealed that CTSG overexpression suppressed CRC cell progression

Indexed as

Colorectal NeoplasmsProto-Oncogene Proteins c-aktCathepsin GCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansProto-Oncogene Proteins c-bcl-2Signal TransductionTOR Serine-Threonine KinasesBCL2 protein, humanCathepsin GCTSG protein, humanMTOR protein, humanProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-bcl-2TOR Serine-Threonine KinasesAktBcl2colorectal cancerCTSGmTOR

Identifiers

PMID37151875
PMCPMC10158020
OpenAlexW4372046977

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.