Evidence map›Paper›PMID 40337959›Full record

ArticleCurrent cancer drug targets2026

CREC Family Genes as Biomarkers and Therapeutic Targets in Lung Adenocarcinoma:

Yimin Jiang, Guangfu Zhu, Xueqin Cheng, Xinyue Mo, Yi Chen, Fengqi Xu, MeiFang Wang, Yijun Tang

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Article in Current cancer drug targets, 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yimin JiangDepartment of Respiratory and Critical Care Medicine, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, Hubei Province, P.R.C, China.
Guangfu ZhuDepartment of General Practice, Sinopharm Dongfeng General Hospital, Hubei University of Medicine, Shiyan, 442000, Hubei Province, P.R.C, China.
Xueqin ChengDepartment of Respiratory and Critical Care Medicine, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, Hubei Province, P.R.C, China.
Xinyue MoDepartment of Respiratory and Critical Care Medicine, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, Hubei Province, P.R.C, China.
Yi ChenDepartment of Respiratory and Critical Care Medicine, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, Hubei Province, P.R.C, China.
Fengqi XuDepartment of Respiratory and Critical Care Medicine, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, Hubei Province, P.R.C, China.
MeiFang WangDepartment of Respiratory and Critical Care Medicine, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, Hubei Province, P.R.C, China.
Yijun TangDepartment of Respiratory and Critical Care Medicine, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, Hubei Province, P.R.C, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung adenocarcinoma (LUAD) is the most common subtype of non-small cell lung cancer (NSCLC), characterized by poor prognosis and limited treatment options. MATERIALS AND

methodsThis study investigated the expression patterns and functional roles of the CREC family genes (RCN1, RCN2, RCN3, SDF2, and CALU) in LUAD using various detailed molecular and in silico experiments.

resultsRT-qPCR analysis revealed significant upregulation of all five genes in LUAD cell lines compared to normal controls, with ROC curve analysis suggesting their potential as diagnostic biomarkers. Validation using independent datasets (Oncomine, UALCAN, and HPA) confirmed these findings at both the transcript and protein levels. Stage-specific expression and promoter methylation analyses demonstrated that RCN1 and CALU exhibit higher expression in advanced stages, while promoter hypomethylation correlated with gene overexpression in LUAD. Mutation and copy number variation (CNV) analyses indicated that CREC gene alterations are common in LUAD, with CALU and RCN3 frequently mutated. Functional assays revealed that knockdown of SDF2 and CALU significantly reduced cell proliferation, colony formation, and wound healing abilities in A549 cells, suggesting their roles in promoting LUAD progression. Gene enrichment and miRNA interaction analyses highlighted the involvement of CREC genes in processes like calcium binding, oxidative stress response, and immune regulation. CALU emerged as a potential prognostic marker, showing a significant association with poorer survival outcomes.

conclusionTogether, the findings of this study suggested that CREC family genes may serve as promising diagnostic and therapeutic targets in LUAD.

Indexed as

Adenocarcinoma of LungBiomarkers, TumorLung NeoplasmsCell ProliferationComputer SimulationDNA MethylationGene Expression Regulation, NeoplasticHumansMicroRNAsPrognosisPromoter Regions, GeneticBiomarkers, TumorMicroRNAsCREC family genesdiagnosisLUADprognosistreatment

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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.