Evidence map›Paper›PMID 37079124›Full record

ArticleMolecular biology reports2023

The validation and clinical significance of LPCAT1 down-regulation in acute myeloid leukemia.

Qin Chen, Zijun Xu, Jiang Lin, Zhaoqun Deng, Jun Qian, Wei Qian

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Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Qin ChenLaboratory Center, Affiliated People's Hospital of Jiangsu University, Zhenjiang, People's Republic of China.
Zijun XuLaboratory Center, Affiliated People's Hospital of Jiangsu University, Zhenjiang, People's Republic of China.
Jiang LinLaboratory Center, Affiliated People's Hospital of Jiangsu University, Zhenjiang, People's Republic of China.
Zhaoqun DengLaboratory Center, Affiliated People's Hospital of Jiangsu University, Zhenjiang, People's Republic of China.
Jun QianDepartment of Hematology, Affiliated People's Hospital of Jiangsu University, Zhenjiang, People's Republic of China. qianjun0007@hotmail.com.
Wei QianLaboratory Center, Affiliated People's Hospital of Jiangsu University, Zhenjiang, People's Republic of China. qian.wei@ufh.com.cn.
Affiliated Hospital of Jiangsu University · CNJiangsu University · CN

Funding

National Natural Science Foundation of China 81970118the Youth Medical Talents Project of "Ke Jiao Qiang Wei" project of Jiangsu province QNRC2016449Zhenjiang Clinical Research Center of Hematology SS2018009
6 · The paper itself

Abstract

backgroundOverexpression of lysophosphatidylcholine acyltransferase 1 (LPCAT1) has been found in various solid cancers and is associated with disease progression, metastasis, and recurrence. However, the expression pattern of LPCAT1 in acute myeloid leukemia (AML) bone marrow remains unknown. The present study aimed to compare LPCAT1 expression differences in bone marrow samples from AML patients and healthy controls and assess the clinical relevance of LPCAT1 in AML. METHODS AND

resultsLPCAT1 expression in bone marrow was significantly lower in AML than in healthy controls predicted by public databases. Furthermore, real-time quantitative PCR (RQ-PCR) validated that LPCAT1 expression in bone marrow was significantly down-regulated in AML compared to healthy controls [0.056 (0.000-0.846) vs 0.253 (0.031-1.000)]. The DiseaseMeth version 2.0 and The Cancer Genome Atlas analysis revealed that the LPCAT1 promoter was hypermethylated in AML, and there was a strong negative correlation between LPCAT1 expression and methylation (R = - 0.610, P < 0.001). RQ-PCR revealed that the frequency of LPCAT1 low expression was lower in the FAB-M4/M5 subtype than in the other subtypes (P = 0.018). The ROC curve revealed that LPCAT1 expression could serve as a potential diagnostic marker for differentiating AML from controls with an area under the ROC curve of 0.819 (95% CI 0.743-0.894, P < 0.001). In cytogenetically normal AML, patients with LPCAT1 low expression had significantly longer overall survival than those without LPCAT1 low expression (median 19 versus 5.5 months, P = 0.036).

conclusionsLPCAT1 is down-regulated in AML bone marrow, and LPCAT1 down-regulation could be used as a potential biomarker for AML diagnosis and prognosis.

Indexed as

Clinical RelevanceLeukemia, Myeloid, Acute1-Acylglycerophosphocholine O-AcyltransferaseBone MarrowDown-RegulationHumansROC Curve1-Acylglycerophosphocholine O-AcyltransferaseLpcat1 protein, humanAcute myeloid leukemiaBone marrowDown-regulationLPCAT1Prognosis

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PMID37079124
OpenAlexW4366464156

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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.