Evidence map›Paper›PMID 34630697›Full record

ArticleExperimental and therapeutic medicine2021

MEX3A knockdown inhibits the tumorigenesis of colorectal cancer via modulating CDK2 expression.

Xin Zhou, Shaojie Li, Tiexiang Ma, Jian Zeng, Huanyu Li, Xiang Liu, Feng Li, Bin Jiang, Ming Zhao, Zhuo Liu and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Experimental and therapeutic medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Xin ZhouDepartment of General Surgery, Xiangtan Central Hospital, Xiangtan, Hunan 411100, P.R. China.
Shaojie LiDepartment of General Surgery, Xiangtan Central Hospital, Xiangtan, Hunan 411100, P.R. China.
Tiexiang MaDepartment of General Surgery, Xiangtan Central Hospital, Xiangtan, Hunan 411100, P.R. China.
Jian ZengDepartment of General Surgery, Xiangtan Central Hospital, Xiangtan, Hunan 411100, P.R. China.
Huanyu LiDepartment of General Surgery, Xiangtan Central Hospital, Xiangtan, Hunan 411100, P.R. China.
Xiang LiuDepartment of General Surgery, Xiangtan Central Hospital, Xiangtan, Hunan 411100, P.R. China.
Feng LiDepartment of General Surgery, Xiangtan Central Hospital, Xiangtan, Hunan 411100, P.R. China.
Bin JiangDepartment of General Surgery, Xiangtan Central Hospital, Xiangtan, Hunan 411100, P.R. China.
Ming ZhaoDepartment of General Surgery, Xiangtan Central Hospital, Xiangtan, Hunan 411100, P.R. China.
Zhuo LiuDepartment of General Surgery, Xiangtan Central Hospital, Xiangtan, Hunan 411100, P.R. China.
Yiyu QinClinical Medical College, Follow-up Research Center, Jiangsu Vocational College of Medicine, Yancheng, Jiangsu 224005, P.R. China.
Xiangyang Central Hospital · CNJiangsu Vocational College of Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is a malignant tumor of the gastrointestinal tract and a leading cause of cancer-associated mortality worldwide. Mex-3 RNA binding family member A (MEX3A) promotes the progression of multiple types of cancer, including ovarian and cervical cancer. However, to the best of our knowledge, the role of MEX3A in CRC is not completely understood. Therefore, the present study aimed to investigate the function of MEX3A in CRC. The mRNA and protein expression levels of MEX3A in CRC cells were analyzed using reverse transcription-quantitative PCR and western blotting, respectively. Cell Counting Kit-8 assays were used to measure cell viability. Cell apoptosis and cell cycle distribution were detected via flow cytometry, and CRC cell invasion was analyzed by performing Transwell assays. Moreover, the mitochondrial membrane potential in CRC cells was measured via JC-1 staining. The results of the present study revealed that the expression levels of MEX3A were upregulated in CRC tissues compared with adjacent healthy tissues. MEX3A knockdown notably inhibited CRC cell viability, and induced apoptosis and mitochondrial injury. In addition, MEX3A knockdown markedly induced G

Indexed as

CDK2cell apoptosiscolorectal cancermex-3 RNA binding family member A

Identifiers

PMID34630697
PMCPMC8495542
OpenAlexW3201146882

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Registered trials

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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.