Evidence map›Paper›PMID 41681464›Full record

ArticleAnimals : an open access journal from MDPI2026

miR-215-5p Suppresses Proliferation/Cell-Cycle Progression and Promotes Apoptosis via Targeting CTCF in Goat Mammary Epithelial Cells.

Sijiang Liu, Hongxin Sun, Manhong Wei, Jiangtao Huang, Zilong Guo, Yujie Han, Xian Qiao, Hongqiang Li, Huaiping Shi, Baolong Liu and 1 more

Abstract read
In one paragraph

Article in Animals : an open access journal from MDPI, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Sijiang LiuHebei Key Laboratory of Specialty Animal Germplasm Resources Exploration and Innovation, College of Animal Science and Technology, Hebei Normal University of Science &Technology, Qinhuangdao 066600, China.
Hongxin SunHebei Institute of Animal Science and Veterinary Medicine, Baoding 071000, China.
Manhong WeiHebei Key Laboratory of Specialty Animal Germplasm Resources Exploration and Innovation, College of Animal Science and Technology, Hebei Normal University of Science &Technology, Qinhuangdao 066600, China.
Jiangtao HuangState Key Laboratory of Cancer Biology, Department of Physiology and Pathophysiology, School of Basic Medical Science, Air Force Medical University, Xi'an 710032, China.
Zilong GuoHebei Key Laboratory of Specialty Animal Germplasm Resources Exploration and Innovation, College of Animal Science and Technology, Hebei Normal University of Science &Technology, Qinhuangdao 066600, China.
Yujie HanHebei Key Laboratory of Specialty Animal Germplasm Resources Exploration and Innovation, College of Animal Science and Technology, Hebei Normal University of Science &Technology, Qinhuangdao 066600, China.
Xian QiaoHebei Key Laboratory of Specialty Animal Germplasm Resources Exploration and Innovation, College of Animal Science and Technology, Hebei Normal University of Science &Technology, Qinhuangdao 066600, China.
Hongqiang LiHebei Key Laboratory of Specialty Animal Germplasm Resources Exploration and Innovation, College of Animal Science and Technology, Hebei Normal University of Science &Technology, Qinhuangdao 066600, China.
Huaiping ShiCollege of Animal Science and Technology, Northwest A&F University, Yangling 712100, China.
Baolong LiuCollege of Animal Science and Technology, Northwest A&F University, Yangling 712100, China.
Yuexin ShaoHebei Key Laboratory of Specialty Animal Germplasm Resources Exploration and Innovation, College of Animal Science and Technology, Hebei Normal University of Science &Technology, Qinhuangdao 066600, China.

Funding

Discipline Research Foundation of Hebei Normal University of Science and Technology 2025YB012National Natural Science Foundation of China 32272828Natural Science Foundation of Hebei Province C2025407018the earmarked fund for Hebei Agriculture Research System HARS
6 · The paper itself

Abstract

MicroRNA (miRNA) is a type of small non-coding RNA that influences various biological processes by targeting gene expression. However, the roles of microRNA in mediating ruminant mammary cell proliferation and survival remain poorly understood. This study aimed to elucidate how miR-215-5p regulates cell cycle and apoptosis-related genes in goat mammary epithelial cells (GMECs). The effects of miR-215-5p on cell cycle and apoptosis were assessed by flow cytometry. A combination of bioinformatics analysis was conducted to predict the target genes of miR-215-5p; this was followed by experimental validation using techniques such as luciferase reporter assays. The effects of CTCF, the targeting gene of miR-215-5p, on cell cycle and apoptosis were examined by qRT-PCR, Western blot and flow cytometry in GMECs. The study demonstrated that miR-215-5p induced cell-cycle arrest at the G0/G1 phase and promoted apoptosis in GMECs. Mechanistically, miR-215-5p downregulated CTCF expression by directly targeting its 3'-untranslated region (3'UTR). This miR-215-5p-mediated depletion of CTCF inhibits CDK2 and CDK6 activity, consequently downregulating genes involved in cell-cycle progression. Furthermore, the miR-215-5p/CTCF axis was found to promote apoptosis by downregulating the protein expression of Bcl-xL and upregulating the gene expression of Bax. In summary, miR-215-5p suppresses GMEC proliferation and survival through CTCF-dependent histone modifications.

Indexed as

apoptosiscell cycleCTCFgoat mammary epithelial cellsmiR-215-5p

Identifiers

PMID41681464
PMCPMC12897051

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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.