Heat shock protein 27: a potential biomarker of peritoneal metastasis in epithelial ovarian cancer?

Tumor Biology ◽  
2013 ◽  
Vol 35 (2) ◽  
pp. 1051-1056 ◽  
Author(s):  
M. Zhao ◽  
J. X. Ding ◽  
K. Zeng ◽  
J. Zhao ◽  
F. Shen ◽  
...  
2012 ◽  
Vol 19 (7) ◽  
pp. 748-753 ◽  
Author(s):  
M. Zhao ◽  
F. Shen ◽  
Y. X. Yin ◽  
Y. Y. Yang ◽  
D. J. Xiang ◽  
...  

Author(s):  
Dominique Könsgen ◽  
Gerd Klinkmann ◽  
Anne Kaul ◽  
Karoline Diesing ◽  
Jalid Sehouli ◽  
...  

2008 ◽  
Vol 54 (1) ◽  
pp. 139-146 ◽  
Author(s):  
Isabella Kardys ◽  
Nader Rifai ◽  
Olivier Meilhac ◽  
Jean-Baptiste Michel ◽  
Jose Luis Martin-Ventura ◽  
...  

Abstract Background: Heat shock protein 27 (HSP27) has been hypothesized to be a potential biomarker of atherothrombosis. However, no prospective studies have yet been performed to investigate the association between HSP27 plasma concentration and incident cardiovascular events among initially healthy individuals. Methods: We evaluated plasma concentrations of HSP27 at baseline among 255 initially healthy participants in the Women’s Health Study who subsequently developed myocardial infarction, ischemic stroke, or cardiovascular death during a follow-up period of up to 5.9 years and among an equal number of women matched for age and smoking but who remained free of cardiovascular disease over the same time period. Results: Overall, HSP27 plasma concentrations were inversely associated with age (Spearman correlation coefficient r = −0.258, P <0.001), but not with other established cardiovascular risk factors. Conditional logistic regression analysis showed no significant association of baseline HSP27 plasma concentration with future cardiovascular disease; the odds ratio for upper vs lower tertile of HSP27 concentration at baseline was 0.99 (95% CI 0.62–1.57, P for trend = 0.99). Conclusion: In this prospective study of initially healthy women, baseline HSP27 plasma concentration was not associated with incident cardiovascular events.


2017 ◽  
Vol 2017 ◽  
pp. 1-12 ◽  
Author(s):  
Matthias B. Stope ◽  
Gerd Klinkmann ◽  
Karoline Diesing ◽  
Dominique Koensgen ◽  
Martin Burchardt ◽  
...  

The heat shock protein HSP27 has been correlated in ovarian cancer (OC) patients with aggressiveness and chemoresistance and, therefore, represents a promising potential biomarker for OC diagnosis, prognosis, and treatment response. Notably, secretion of soluble HSP27 has been described by a few cell types and may take place as well in OC cells. Therefore, we studied HSP27 secretion mechanisms under diverse cellular conditions in an OC cell model system. Secretion of HSP27 was characterized after overexpression of HSP27 by transfected plasmids and after heat shock. Intra- and extracellular HSP27 amounts were assessed by Western blotting and ELISA. Protein secretion was blocked by brefeldin A and the impact of the HSP27 phosphorylation status was analyzed overexpressing HSP27 phosphomutants. The present study demonstrated that HSP27 secretion by OVCAR-3 and SK-OV-3 cells depends on intracellular HSP27 concentrations. Moreover, HSP27 secretion is independent of the endoplasmic reticulum secretory pathway and HSP27 phosphorylation. Notably, analysis of OC cell-born exosomes not only confirmed the concentration-dependent correlation of HSP27 expression and secretion but also demonstrated a concentration-dependent incorporation of HSP27 protein into exosomes. Thus, secreted HSP27 may become more important as an extracellular factor which controls the tumor microenvironment and might be a noninvasive biomarker.


Oncotarget ◽  
2017 ◽  
Vol 9 (2) ◽  
pp. 1602-1616 ◽  
Author(s):  
Janice M. Santiago-O’Farrill ◽  
Eugenie S. Kleinerman ◽  
Mario G. Hollomon ◽  
Andrew Livingston ◽  
Wei-Lien Wang ◽  
...  

2010 ◽  
Vol 18 (12) ◽  
pp. 1237
Author(s):  
Wei-Jie Liu ◽  
Huan-Long Qin ◽  
Yan-Lei Ma ◽  
Jia-Yuan Peng

2016 ◽  
Vol 76 (10) ◽  
Author(s):  
M Weiss ◽  
MB Stope ◽  
G Klinkmann ◽  
D Könsgen ◽  
S Brucker ◽  
...  

1993 ◽  
Vol 11 (5) ◽  
pp. 891-898 ◽  
Author(s):  
E Kimura ◽  
R E Enns ◽  
J E Alcaraz ◽  
J Arboleda ◽  
D J Slamon ◽  
...  

PURPOSE Ovarian carcinomas express the 60-kD heat-shock protein HSP-60 at widely varying levels in different tumors. The aim of this study was to determine whether there was a relationship between expression of HSP-60 and survival in patients with ovarian carcinoma. MATERIALS AND METHODS Total RNA and DNA were prepared from 51 epithelial ovarian cancer tissue samples. The expression and structure of the HSP-60 gene were examined by Northern and Southern blot analyses using the carboxyl-terminal portion of this gene as a probe (0.89 kilobases [kb]). HSP-60 expression was correlated with overall survival by the Kaplan-Meier method. RESULTS The 2.3-kb HSP-60 message was detected in all samples, but there was marked variation from tumor to tumor. Patients were classified into two groups on the basis of HSP-60 expression: group 1 (n = 25) included patients with low expression, and group 2 (n = 26) consisted of patients with high expression. There were no significant differences between the groups with respect to age, cell type, pathologic grade, clinical stage, and previous treatment. After a median follow-up period of 17 months, Kaplan-Meier plots demonstrated a much better survival for group 1 (median, 46.8 months; 41% at 4 years) than group 2 (median, 22.1 months; 16% at 3.9 years), a difference that was highly significant by the Mantel-Haenszel test (P = .00183). Southern blot analysis of these samples showed no amplification or rearrangement of the gene. CONCLUSION The level of HSP-60 mRNA expression is a valuable prognostic factor in epithelial ovarian cancer. Variation in the level of expression is not due to amplification of this gene.


2021 ◽  
Author(s):  
Shahan Mamoor

Epithelial ovarian cancer (EOC) is the most lethal gynecologic cancer (1). We performed discovery of genes associated with epithelial ovarian cancer and of the high-grade serous ovarian cancer (HGSC) subtype, using published microarray data (2, 3) to compare global gene expression profiles of normal ovary or fallopian tube with that of primary tumors from women diagnosed with epithelial ovarian cancer or HGSC. We identified the gene encoding heat shock protein family B (small) member 3, HSPB3, as among the genes whose expression was most different in epithelial ovarian cancer as compared to the normal fallopian tube. HSPB3 expression was significantly lower in high-grade serous ovarian tumors relative to normal fallopian tube. HSPB3 expression correlated with progression-free survival in patients with p53 mutant ovarian cancer. These data indicate that expression of HSPB3 is perturbed in epithelial ovarian cancers broadly and in ovarian cancers of the HGSC subtype. HSPB3 may be relevant to pathways underlying ovarian cancer initiation (transformation) or progression.


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