Evidence map›Paper›PMID 40797188›Full record

ArticleBMC gastroenterology2025

Overexpression of Protein Kinase C iota as a prognostic marker and its role in oxaliplatin resistance in colorectal cancer.

Xuankai Liao, Mengyuan Liu, Chunli Hong, Yuyan Liu, Qing Li, Ying Chen, Tingzhen Zhang, Hongda Chen, Shuying Fu

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Article in BMC gastroenterology, 2025. 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

9 authors.

Xuankai LiaoDepartment of Pathology, The Seventh Affiliated Hospital, Sun Yat-sen University, Zhenyuan road No. 628, 518107, Shenzhen, China.
Mengyuan LiuDepartment of dermatology, The Seventh Affiliated Hospital, Sun Yat-sen University, Zhenyuan Road 628, Shenzhen, 518107, China.
Chunli HongDepartment of dermatology, The Seventh Affiliated Hospital, Sun Yat-sen University, Zhenyuan Road 628, Shenzhen, 518107, China.
Yuyan LiuDepartment of dermatology, The Seventh Affiliated Hospital, Sun Yat-sen University, Zhenyuan Road 628, Shenzhen, 518107, China.
Qing LiDepartment of dermatology, The Seventh Affiliated Hospital, Sun Yat-sen University, Zhenyuan Road 628, Shenzhen, 518107, China.
Ying ChenDepartment of Traditional Chinese Medicine, Shenzhen Longhua Maternity and Child Healthcare Hospital, Shenzhen, 510108, China.
Tingzhen Zhang *Department of Pathology, The Seventh Affiliated Hospital, Sun Yat-sen University, Zhenyuan road No. 628, 518107, Shenzhen, China. zhangtingzhen@sysush.com.
Hongda Chen *Department of Traditional Chinese Medicine, The Seventh Affiliated Hospital, Sun Yat-sen University, Zhenyuan road No. 628, 518107, Shenzhen, China. chenhongda@sysush.com.
Shuying Fu *Department of dermatology, The Seventh Affiliated Hospital, Sun Yat-sen University, Zhenyuan Road 628, Shenzhen, 518107, China. fushuying@sysush.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProtein Kinase C iota (PKCι) has been implicated in cancer progression and chemoresistance, but its prognostic significance in solid tumors remains unclear. This study aimed to evaluate the expression of PKCι in tumor tissues and its association with clinicopathological features, survival outcomes, and chemotherapy response in patients with cancer.

methodsA retrospective analysis was conducted on patients with confirmed cancer diagnoses. Immunohistochemistry (IHC) was used to assess PKCι expression levels in tumor tissues. Kaplan-Meier survival curves and univariate Cox analysis were applied to evaluate the impact of PKCι expression and other clinicopathological variables on overall survival (OS) and progression-free survival (PFS). The association between PKCι expression and chemotherapy resistance, particularly oxaliplatin resistance, was also investigated.

resultsPKCι overexpression was possibly correlated with advanced clinical stage, metastasis, organs involvement, vascular invasion, and perineural invasion. Patients with PKCι overexpression was possibly correlated with oxaliplatin resistance(P = 0.014). Besides, Patients with PKCι overexpression exhibited significantly shorter PFS compared to those with low expression levels (P = 0.0006). Univariate Cox analysis confirmed that metastasis (H.R. = 11.910, P = 0.018) and clinical staging (H.R. = 5.498, P = 0.027) were independent prognostic factors for OS, whereas CEA levels (H.R. = 3.497, P = 0.005) was independent predictors of PFS.

conclusionPKCι overexpression is associated with tumor aggressiveness and chemotherapy resistance, indicating its potential as a prognostic biomarker and therapeutic target in cancer preliminarily.

Indexed as

Antineoplastic AgentsBiomarkers, TumorColorectal NeoplasmsDrug Resistance, NeoplasmOxaliplatinProtein Kinase CAdultAgedFemaleHumansImmunohistochemistryIsoenzymesKaplan-Meier EstimateMaleMiddle AgedPrognosisAntineoplastic AgentsBiomarkers, TumorIsoenzymesOxaliplatinProtein Kinase CProtein Kinase C-lambdaCancer prognosisMetastasisOverall survivalOxaliplatin resistancePKCιProgression-free survivalVascular invasion

Identifiers

PMID40797188
PMCPMC12341243

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