» Articles » PMID: 21416470

Over-expression of LAPTM4B is Associated with Poor Prognosis and Chemotherapy Resistance in Stages III and IV Epithelial Ovarian Cancer

Overview
Journal J Surg Oncol
Date 2011 Mar 19
PMID 21416470
Citations 32
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The purpose of this study was to determine whether LAPTM4B over-expression is associated with the prognosis and chemotherapy resistance in patients with stages III and IV epithelial ovarian carcinoma, i.e., patients with peritoneal metastasis or lymph node metastasis of epithelial ovarian carcinoma.

Methods: LAPTM4B expression was evaluated in 10 normal ovarian and 113 stages III-IV ovarian carcinomas specimens by Western blotting analyses and immunohistochemistry. Univariate and multivariate analyses were performed to determine the association between LAPTM4B expression and prognosis and the relationship between LAPTM4B over-expression and chemotherapy resistance.

Results: Western blotting analysis demonstrated that LAPTM4B was overexpressed in ovarian cancers, and immunohistochemistry results revealed that 80 patients were LAPTM4B over-expression. The five-year overall survival (OS) rates for patients with high LAPTM4B expression and low LAPTM4B expression were 27.36% and 90.7%, respectively (hazard ratio = 20.611, 95% CI: 5.916-71.808, P < 0.0001). The five-year progression-free survival (PFS) rate was 17.68% for patients in the high-expression group and 84.42% for patients in the low-expression group (hazard ratio = 17.852, 95% CI: 6.31-5.935, P < 0.0001); The presence of chemotherapy resistance was significantly associated with LAPTM4B expression (OR: 36.609, 95% CI: 4.737-282.941, P = 0.0006).

Conclusions: LAPTM4B over-expression is an independent factor in stages III-IV epithelial ovarian carcinoma prognosis and chemotherapy resistance, and it may be an important potential biomarker.

Citing Articles

LAPTM4B-mediated hepatocellular carcinoma stem cell proliferation and MDSC migration: implications for HCC progression and sensitivity to PD-L1 monoclonal antibody therapy.

Wang H, Zhou Q, Xie D, Xu Q, Yang T, Wang W Cell Death Dis. 2024; 15(2):165.

PMID: 38388484 PMC: 10884007. DOI: 10.1038/s41419-024-06542-8.


Advance in vasculogenic mimicry in ovarian cancer (Review).

Tian X, Si Q, Liu M, Shi J, Zhao R, Xiong Y Oncol Lett. 2023; 26(4):456.

PMID: 37736556 PMC: 10509778. DOI: 10.3892/ol.2023.14043.


Serum LAPTM4B as a Potential Diagnostic and Prognostic Biomarker for Breast Cancer.

Wang L, Wang Y, Zhang Q Biomed Res Int. 2022; 2022:6786351.

PMID: 36506911 PMC: 9729050. DOI: 10.1155/2022/6786351.


Systematic Pan-Cancer Analysis and Experimental Verification Identify FOXA1 as an Immunological and Prognostic Biomarker in Epithelial Ovarian Cancer.

Wang K, Guan C, Yu J, Chen X, Shang X, Mei S Dis Markers. 2022; 2022:9328972.

PMID: 36393971 PMC: 9646314. DOI: 10.1155/2022/9328972.


FOXA1 can be modulated by HDAC3 in the progression of epithelial ovarian carcinoma.

Lou T, Liu C, Qu H, Zhang Z, Wang S, Zhuang H J Transl Med. 2022; 20(1):19.

PMID: 34991620 PMC: 8740004. DOI: 10.1186/s12967-021-03224-3.