Evidence map›Paper›PMID 41450965›Full record

ReviewFrontiers in molecular biosciences2025

Targeting microRNA-143 in colorectal cancer: advances in molecular biosciences for biomarker-based diagnostics, therapeutic strategies, and drug resistance prediction.

Xue Wang, Lei Wang, Long Ke

Abstract readReview
In one paragraph

Review in Frontiers in molecular biosciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. miR-143-5p as a Prognostic Biomarker in Colorectal Cancer: Inhibition of Tumor Progression Through Targeting MYCBP.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2026
    Article
  2. Review
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

3 authors.

Xue WangDepartment of Oncology, Mianyang Fulin Hospital, Mianyang Fulin Hospital Co., Ltd., Mianyang, China.
Lei WangSecond Department of Gastrocolorectal Surgery, Jilin Cancer Hospital, Changchun, Jilin, China.
Long KeDepartment of Health Examination, The Third Affiliated Hospital of Shanghai University, Wenzhou No.3 Clinical Institute Affiliated to Wenzhou Medical University, Wenzhou People's Hospital, Wenzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) persists as a significant global health challenge, distinguished by intricate molecular modifications and a notable propensity for resistance to standard therapeutic interventions. Among the regulatory factors contributing to CRC pathogenesis, microRNAs (miRNAs) have emerged as pivotal regulators of gene expression, presenting innovative prospects for diagnostic and therapeutic advancements. Notably, microRNA-143 (miR-143) has attracted considerable attention as a tumor-suppressive miRNA, exhibiting diverse functions in the development, progression, and therapeutic response of CRC. This review delineates an exhaustive examination of the molecular mechanisms by which miR-143 modulates critical oncogenic pathways, encompassing KRAS signaling, epithelial-mesenchymal transition, and metabolic reprogramming. We underscore recent progress in the molecular biosciences that position miR-143 as a promising biomarker for the early detection and prognosis of CRC. Furthermore, we investigate its emergent function in the modulation of sensitivity to chemotherapeutic and targeted therapeutic agents, emphasizing its potential utility in predicting and mitigating drug resistance in CRC cells. By synthesizing contemporary findings within the domains of molecular diagnostics and therapeutic interventions, this review accentuates the clinical potential of targeting miR-143 in the personalized management of CRC and the prediction of drug resistance.

Indexed as

colorectal cancerdrug resistancemir-143molecular diagnosticsnon-coding RNAs

Identifiers

PMID41450965
PMCPMC12727956

What OpenQuestion holds

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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.