Evidence map›Paper›PMID 40302069›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2025

Role of microRNA-486-5p as Biomarker Response in Cell Line K562 of Chronic Myeloid Leukemia.

Jay Prakash Jha, Dinesh Kumar Sinha, Sanjeet Singh, Rekha Kumari

Abstract read
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Article in Asian Pacific journal of cancer prevention : APJCP, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Jay Prakash JhaDepartment of Biochemistry, Indira Gandhi Institute of Medical Sciences, Patna, India.ORCID 0009-0004-4011-4755
Dinesh Kumar SinhaDepartment of Oncology, Indira Gandhi Institute of Medical Sciences, Patna, India.ORCID 0000-0002-4454-8989
Sanjeet SinghDepartment of Pathology and Lab Medicine, AIIMS, Deoghar, India.
Rekha KumariDepartment of Biochemistry, Indira Gandhi Institute of Medical Sciences, Patna, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aims to evaluate the efficiency and accuracy of microRNA (miR)-486-5p as a screening and diagnostic tool for chronic myeloid leukemia (CML).

methodsThe study was performed on K562 cell line. The cell line of the erythroleukemia type originated from a 53-year-old female patient suffering from chronic myelogenous leukemia during a blast crisis. The cells are non-adherent, rounded in shape, and positive for the BCR: ABL1 fusion gene. In addition, we measured the expression of miR-486-5p in peripheral blood monocytes from healthy volunteers and compared the result with Imatinib treated and untreated K562 cell line.

resultAs compared to control blood cells from healthy volunteers, there was a statistically significant downregulation of the expression of miR-486-5p in untreated K562 cells (p-value = 0.007). After Imatinib exposure, the miR-486-5p expression was significantly upregulated in K562 cells as compared to treated and untreated K562 cells (p-value = 0.004).

conclusionNumerous reports demonstrate the role of miRNA in acting as oncogenes or tumor suppressors in various cancers. We have reported an alteration in the expression of miR-486-5p in the CML cell line. The upregulation of miR-486-5p expression in the post-imatinib exposure K562 cell line suggests that miR-486-5p has an onco-suppressor effector role in the BCR-ABL downstream signalling pathway. It is possible to investigate miR-486-5p as a potential biomarker for early CML detection.

Indexed as

Biomarkers, TumorLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMicroRNAsAntineoplastic AgentsCase-Control StudiesCell ProliferationFemaleFusion Proteins, bcr-ablHumansImatinib MesylateK562 CellsMiddle AgedTumor Cells, CulturedAntineoplastic AgentsBiomarkers, TumorFusion Proteins, bcr-ablImatinib MesylateMicroRNAsMIRN486 microRNA, humanBCR-ABL1K562 cell lineKeywords - CMLmiR-486-5p expression

Identifiers

PMID40302069
PMCPMC12227951

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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.