Evidence map›Paper›PMID 36008699›Full record

ArticleBiochemical genetics2023

CISD2 Promotes Proliferation of Colorectal Cancer Cells by Inhibiting Autophagy in a Wnt/β-Catenin-Signaling-Dependent Pathway.

Jie Wang, Jun Hu, Mingyun Wang, Huaqin Yuan, Yajun Xing, Xiaohua Zhou, Meiqing Ding, Wenqiang Chen, Baoqi Qu, Liangxue Zhu

Abstract read
PubMed Publisher
In one paragraph

Article in Biochemical genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Hesperetin Alleviates Bleomycin-Induced Pulmonary Fibrosis by Modulating Cellular Senescence and Promoting Impaired Autophagy in a CISD2-Dependent Manner.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  3. Review
  4. Article
  5. Article
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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

10 authors at 1 institution in 1 country.

Jie Wang *Department of Oncology, Gaochun People's Hospital, No. 53, Maoshan Road, Nanjing, 211300, Jiangsu, China.
Jun Hu *Department of Oncology, Gaochun People's Hospital, No. 53, Maoshan Road, Nanjing, 211300, Jiangsu, China.
Mingyun WangDepartment of Oncology, Gaochun People's Hospital, No. 53, Maoshan Road, Nanjing, 211300, Jiangsu, China. mingy_ww@163.com.ORCID http://orcid.org/0000-0002-1252-3816
Huaqin YuanDepartment of Oncology, Gaochun People's Hospital, No. 53, Maoshan Road, Nanjing, 211300, Jiangsu, China.
Yajun XingDepartment of Oncology, Gaochun People's Hospital, No. 53, Maoshan Road, Nanjing, 211300, Jiangsu, China.
Xiaohua ZhouDepartment of Gastrointestinal Surgery, Gaochun People's Hospital, Nanjing, 211300, Jiangsu, China.
Meiqing DingDepartment of Oncology, Gaochun People's Hospital, No. 53, Maoshan Road, Nanjing, 211300, Jiangsu, China.
Wenqiang ChenDepartment of Oncology, Gaochun People's Hospital, No. 53, Maoshan Road, Nanjing, 211300, Jiangsu, China.
Baoqi QuDepartment of Oncology, Gaochun People's Hospital, No. 53, Maoshan Road, Nanjing, 211300, Jiangsu, China.
Liangxue ZhuDepartment of Oncology, Gaochun People's Hospital, No. 53, Maoshan Road, Nanjing, 211300, Jiangsu, China.
Gaochun People's Hospital · CN

Funding

2014 Medical Clinical Science and Technology Development Fund of Jiangsu University JLY201440087
6 · The paper itself

Abstract

The aim of this study is to investigate the role of CDGSH iron-sulfur domain 2 (CISD2) in colorectal cancer (CRC). The purpose of this study was to investigate the role of CDGSH iron-sulfur domain 2 (CISD2) in colorectal cancer (CRC) progression. The expression of CISD2 in CRC cell lines was measured by western blotting. Functional assays including MTT assays and colony formation assays were performed to explore the role of CISD2 in regulating tumor growth. Flow cytometry analysis was used to examine the percentage of apoptotic CRC cells. Expression of apoptosis-related gene, autophagy-related markers, and the protein included in Wnt/β-Catenin signaling was also determined by western blotting. The in vivo role of CISD2 was also examined in a xenograft model. CISD2 expression was significantly increased in CRC cells. CISD2 promoted the CRC cell proliferation and inhibited the apoptosis and autophagy of CRC cells. Moreover, knockdown of CISD2 inhibited the activation of Wnt/β-Catenin-signaling pathway. Knockdown of CISD2 inhibited the tumor growth in nude mice. CISD2 promoted colorectal cancer development by inhibiting CRC cell apoptosis and autophagy depending on activating Wnt/β-Catenin-signaling pathway.

Indexed as

beta CateninColorectal NeoplasmsAnimalsAutophagyCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHumansIronMiceMice, NudeSulfurXenograft Model Antitumor Assaysbeta CateninIronSulfurApoptosisAutophagyCISD2Colorectal cancerWnt/β-Catenin pathway

Identifiers

PMID36008699
OpenAlexW4293240330

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.