Evidence map›Paper›PMID 33273855›Full record

ArticleCancer management and research2020

MicroRNA-1276 Promotes Colon Cancer Cell Proliferation by Negatively Regulating LACTB.

Chunxiao Wang, Zesheng Shi, Zhongshi Hong, Jianpeng Pan, Zhichuan Chen, Chengzhi Qiu, Haibin Zhuang, Xuecong Zheng

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
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  4. The Pivotal Role of LACTB in the Process of Cancer Development.International journal of molecular sciences · 2025
    Review
  5. Article
  6. miR-125b-5p, miR-155-3p, and miR-214-5p and TargetInternational journal of molecular sciences · 2023
    Article
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  8. 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

8 authors at 2 institutions in 1 country.

Chunxiao Wang *Department of General Surgery, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, People's Republic of China.
Zesheng Shi *Department of General Surgery, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, People's Republic of China.
Zhongshi HongDepartment of General Surgery, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, People's Republic of China.
Jianpeng PanDepartment of General Surgery, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, People's Republic of China.
Zhichuan ChenDepartment of General Surgery, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, People's Republic of China.
Chengzhi QiuDepartment of General Surgery, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, People's Republic of China.
Haibin ZhuangDepartment of General Surgery, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, People's Republic of China.
Xuecong ZhengDepartment of General Surgery, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, People's Republic of China.
Fujian Medical University · CNSecond Affiliated Hospital of Fujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeLACTB, regulated by a variety of microRNAs (miRNAs), is proven to be a tumor suppressor. However, there are few reports that LACTB in colon cancer cells is regulated by miRNA. Therefore, the aim of this study was to explore the miRNAs that regulate LACTB in colon cancer. PATIENTS AND

methodsData from TCGA were analyzed in starBase and GEPIA2, and Western blot and quantitative PCR (qPCR) were used to detect the expression of LACTB in colon cancer cell lines. MiRNAs targeting LACTB were predicted by MicroT-CDS, starBase, miRDB, mirDIP, and DIANA. The relationship between LACTB and miRNA was explored by dual-luciferase assay. MTT, propidium iodide (PI), Western blot, Annexin V-FITC/PI Kit, qPCR and transwell assay were used to detect the changes in cell proliferation, cell cycle, autophagy, apoptosis, epithelial-to-mesenchymal transition (EMT), cell migration, and invasiveness in colon cancer cells that overexpressed miR-1276 and/or LACTB.

resultsThe results showed that the LACTB mRNA level was lower and the miR-1276 level was higher in colon cancer than in normal tissue. MiR-1276 inhibited the expression of LACTB. Furthermore, overexpression of miR-1276 in colon cancer cells increased proliferation, migration, invasiveness and EMT, and decreased autophagy and apoptosis. Supplementing LACTB suppressed these effects of miR-1276.

conclusionIn conclusion, miR-1276, which may be a potential therapy for colon cancer, inhibits cell growth and promotes apoptosis by targeting LACTB in colon cancer cells.

Indexed as

cell proliferationcolonic neoplasmsLACTBmicroRNAmiR-1276

Identifiers

PMID33273855
PMCPMC7705278
OpenAlexW3107765502

What OpenQuestion holds

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LicenceCC BY-NC
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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.