Evidence map›Paper›PMID 37814227›Full record

ArticleBMC cancer2023

CADM1 impairs the effect of miR-1246 on promoting cell cycle progression in chemo-resistant leukemia cells.

Bei Xie, Lei Zhao, Zhewen Zhang, Cunmin Zhou, Ye Tian, Yingying Kang, Jing Chen, Hulai Wei, Linjing Li

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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

9 authors at 2 institutions in 1 country.

Bei Xie *Department of Immunology, School of Basic Medical Sciences, Lanzhou University, No. 199 Donggang West Road, Lanzhou, 730000, Gansu, China. xieb@lzu.edu.cn.
Lei Zhao *Shaanxi Meili Omni-Honesty Animal Health Co., Ltd, Xi'an, 710000, Shaanxi, China.
Zhewen Zhang *Department of Immunology, School of Basic Medical Sciences, Lanzhou University, No. 199 Donggang West Road, Lanzhou, 730000, Gansu, China.
Cunmin ZhouThe First Hospital of Lanzhou University, Lanzhou, 730000, Gansu, China.
Ye TianThe Second Hospital of Lanzhou University, Lanzhou, 730000, Gansu, China.
Yingying KangDepartment of Immunology, School of Basic Medical Sciences, Lanzhou University, No. 199 Donggang West Road, Lanzhou, 730000, Gansu, China.
Jing ChenDepartment of Immunology, School of Basic Medical Sciences, Lanzhou University, No. 199 Donggang West Road, Lanzhou, 730000, Gansu, China.
Hulai WeiDepartment of Immunology, School of Basic Medical Sciences, Lanzhou University, No. 199 Donggang West Road, Lanzhou, 730000, Gansu, China. weihulai@lzu.edu.cn.
Linjing LiThe Second Hospital of Lanzhou University, Lanzhou, 730000, Gansu, China. lilinj@lzu.edu.cn.
Lanzhou University · CNLanzhou University Second Hospital · CN

Funding

Cuiying Scientific and Technological Innovation Program of Lanzhou University Second Hospital CY2021-MS-A20Health Industrial Outstanding Youth Talent Project of Gansu Province GSWSQN2022-02Higher Education Innovation Fund Project of Gansu Province 2021B-021International Technological Cooperation Project of Gansu Province 18YF1WA117National Natural Science Foundation of China 82272405, 82060531, 81602622Natural Science Foundation of Gansu Province 21JR7RA448
6 · The paper itself

Abstract

The interruption of normal cell cycle execution acts as an important part to the development of leukemia. It was reported that microRNAs (miRNAs) were closely related to tumorigenesis and progression, and their aberrant expression had been demonstrated to play a crucial role in numerous types of cancer. Our previous study showed that miR-1246 was preferentially overexpressed in chemo-resistant leukemia cell lines, and participated in process of cell cycle progression and multidrug resistant regulation. However, the underlying mechanism remains unclear. In present study, bioinformatics prediction and dual luciferase reporter assay indicated that CADM1 was a direct target of miR-1246. Evidently decreased expression of CADM1 was observed in relapsed primary leukemia patients and chemo-resistant cell lines. Our results furtherly proved that inhibition of miR-1246 could significantly enhance drug sensitivity to Adriamycin (ADM), induce cell cycle arrest at G0/G1 phase, promote cell apoptosis, and relieve its suppression on CADM1 in K562/ADM and HL-60/RS cells. Interference with CADM1 could reduce the increased drug sensitivity induced by miR-1246 inhibition, and notably restore drug resistance by promoting cell cycle progression and cell survival via regulating CDKs/Cyclins complexes in chemo-resistant leukemia cells. Above all, our results demonstrated that CADM1 attenuated the role of miR-1246 in promoting cell cycle progression and cell survival, thus influencing multidrug resistance within chemo-resistant leukemia cells via CDKs/Cyclins. Higher expression of miR-1246 and lower expression of CADM1 might be risk factors for leukemia.

Indexed as

LeukemiaMicroRNAsCell Adhesion Molecule-1Cell CycleCell Line, TumorCell ProliferationCyclinsDoxorubicinDrug Resistance, NeoplasmHL-60 CellsHumansCADM1 protein, humanCell Adhesion Molecule-1CyclinsDoxorubicinMicroRNAsMIRN1246 microRNA, humanCADM1CDKs/Cyclins axisCell cycleChemo-resistant leukemia cellsmiR-1246

Identifiers

PMID37814227
PMCPMC10561441
OpenAlexW4387459444

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.