Cited by 47Heat shock proteins researchLung Cancer Research StudiesBreast Cancer Treatment Studies

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Prognostic value of the mRNA expression of members of the HSP90 family in non‑small cell lung cancer

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Liu, Kang, Kang, Min, Li, Jixi, Qin, Wen, Wang, Rensheng·2019·Experimental and Therapeutic Medicine

Abstract

The aim of the present study was to investigate the potential prognostic value of members of the heat shock protein (HSP)90 family in non-small cell lung cancer (NSCLC) patients. The mRNA expression profiles of 1,926 NSCLC patients, which was available from the Kaplan-Meier plotter database, were included in the study. High expression of HSP90AA1 mRNA was significantly associated with a poorer rate of overall survival (OS) for all NSCLC patients [hazard ratio (HR), 1.21; 95% confidence interval (CI): 1.06-1.37; P=0.004], as well as for patients with adenocarcinoma (ADE; HR, 1.3; 95% CI: 1.02-1.65; P=0.034), but no significant correlation was identified for squamous cell carcinoma (SCC) patients (HR, 1.08; 95% CI: 0.85-1.38; P=0.51). High expression of HSP90AB1 and HSP90B1 mRNA was significantly associated with poorer rates of OS in lung SCC and ADE patients combined, as well as in lung ADE patients alone. By contrast, high expression of tumor necrosis factor receptor-associated protein 1 (TRAP1) mRNA was significantly associated with improved OS rates in all NSCLC patients combined (HR, 0.88; 95% CI: 0.77-0.99; P=0.041), as well as ADE patients. In stratified survival analysis, a high expression of HSP90AA1, HSP90AB1 and HSP90B1 predicted poor prognosis in stage I NSLCC patients, suggesting that these genes may serve as stage-independent prognostic indicators. As an elevated expression of HSP90AA1, HSP90AB1, HSP90B1 and TRAP1 was associated with poorer OS outcomes in patients with NSCLC, these HSP90 members may be potential prognostic biomarkers and drug targets for the treatment of NSCLC.

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  • HSP90AB1 facilitates tumorigenesis in a spectrum of cancers, including gastric cancer, breast cancer, NSCLC, hepatocellular carcinoma, and head and neck squamous cell carcinoma.

    “Multiple investigations have revealed that HSP90AB1 facilitates tumorigenesis in a spectrum of cancers, including gastric cancer, breast cancer, non-small cell lung cancer (NSCLC), hepatocellular carcinoma, and head and neck squamous cell carcinoma [13–18].”

    From Celastrol attenuates the invasion and migration and augments the anticancer effects of olaparib in prostate cancer (2024) · cites this paper as [15]

    The Discussion reports that high HSP90AB1 mRNA expression was associated with poorer overall survival in patients with lung adenocarcinoma, a type of NSCLC, but not in patients with squamous cell carcinoma. It does not establish that HSP90AB1 facilitates tumorigenesis; the authors say further research is needed to explore the underlying mechanisms. No page number is available in our copy. (LLM, conf=0.88)

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Research works printed but not linked: 45

  1. Siegel, 2016, Cancer statistics, 2016, CA Cancer J Clin, 66, 7, 10.3322/caac.21332 · DOI · Paper page
  2. Torre, 2015, Global cancer statistics, 2012, CA Cancer J Clin, 65, 87, 10.3322/caac.21262 · DOI
  3. Minna, 2002, Focus on lung cancer, Cancer Cell, 1, 49, 10.1016/S1535-6108(02)00027-2 · DOI
  4. Burrows, 2004, Hsp90 activation and cell cycle regulation, Cell Cycle, 3, 1530, 10.4161/cc.3.12.1277 · DOI
  5. Kolosenko, 2014, IL-6 activated JAK/STAT3 pathway and sensitivity to Hsp90 inhibitors in multiple myeloma, Curr Med Chem, 21, 3042, 10.2174/0929867321666140414100831 · DOI
  6. Patel, 2014, Heat shock protein 90 (HSP90) is overexpressed in p16-negative oropharyngeal squamous cell carcinoma, and its inhibition in vitro potentiates the effects of chemoradiation, Cancer Chemother Pharmacol, 74, 1015, 10.1007/s00280-014-2584-8 · DOI
  7. Shi, 2014, Plasma levels of heat shock protein 90 alpha associated with lung cancer development and treatment responses, Clin Cancer Res, 20, 6016, 10.1158/1078-0432.CCR-14-0174 · DOI
  8. Huang, 2014, Expression of Hsp90alpha and cyclin B1 were related to prognosis of esophageal squamous cell carcinoma and keratin pearl formation, Int J Clin Exp Pathol, 7, 1544
  9. Tian, 2014, High expression of heat shock protein 90 alpha and its significance in human acute leukemia cells, Gene, 542, 122, 10.1016/j.gene.2014.03.046 · DOI
  10. McCarthy, 2008, HSP90 as a marker of progression in melanoma, Ann Oncol, 19, 590, 10.1093/annonc/mdm545 · DOI
  11. Záčková, 2013, Hsp90-a potential prognostic marker in CML, Blood Cells Mol Dis, 50, 184, 10.1016/j.bcmd.2012.11.002 · DOI
  12. Hirakawa, 2015, The combination of Hsp90 inhibitor 17AAG and heavy-ion irradiation provides effective tumor control in human lung cancer cells, Cancer Med, 4, 426, 10.1002/cam4.377 · DOI
  13. Johnson, 2015, Phase I/II study of HSP90 inhibitor AUY922 and erlotinib for EGFR-mutant lung cancer with acquired resistance to epidermal growth factor receptor tyrosine kinase inhibitors, J Clin Oncol, 33, 1666, 10.1200/JCO.2014.59.7328 · DOI
  14. Huang, 2018, Distinct prognostic roles of HSPB1 expression in non-small cell lung cancer, Neoplasma, 65, 161, 10.4149/neo_2018_102 · DOI
  15. Schmidt, 2017, Potential therapeutic impact of CD13 expression in non-small cell lung cancer, PLoS One, 12, e0177146, 10.1371/journal.pone.0186280 · DOI
  16. Xie, 2017, Systematic analysis of gene expression alterations and clinical outcomes of adenylate cyclase-associated protein in cancer, Oncotarget, 8, 27216, 10.18632/oncotarget.16111 · DOI
  17. Hou, 2017, Mining expression and prognosis of topoisomerase isoforms in non-small-cell lung cancer by using Oncomine and Kaplan-Meier plotter, PLoS One, 12, e0174515, 10.1371/journal.pone.0174515 · DOI
  18. Győrffy, 2013, Online survival analysis software to assess the prognostic value of biomarkers using transcriptomic data in non-small-cell lung cancer, PLoS One, 8, e82241, 10.1371/journal.pone.0082241 · DOI
  19. Lukas, 2017, State-of-the-art considerations in small cell lung cancer brain metastases, Oncotarget, 8, 71223, 10.18632/oncotarget.19333 · DOI
  20. Calderwood, 2016, Hsp90 in cancer: Transcriptional roles in the nucleus, Adv Cancer Res, 129, 89, 10.1016/bs.acr.2015.08.002 · DOI
  21. Zhang, 2015, Aberrantly upregulated TRAP1 is required for tumorigenesis of breast cancer, Oncotarget, 6, 44495, 10.18632/oncotarget.6252 · DOI
  22. Palmieri, 2014, Heat shock protein 90 is associated with hyperplasia and neoplastic transformation of canine prostatic epithelial cells, J Comp Pathol, 150, 393, 10.1016/j.jcpa.2014.01.006 · DOI
  23. Badowska-Kozakiewicz, 2012, Immunohistochemical evaluation of expression of heat shock proteins HSP70 and HSP90 in mammary gland neoplasms in bitches, Pol J Vet Sci, 15, 209, 10.2478/v10181-011-0135-3 · DOI
  24. Lee, 2015, Differential expression of heat shock protein 90 isoforms in small cell lung cancer, Int J Clin Exp Pathol, 8, 9487
  25. Wong, 2016, Emerging roles of extracellular Hsp90 in cancer, Adv Cancer Res, 129, 141, 10.1016/bs.acr.2016.01.001 · DOI
  26. Sims, 2011, Extracellular heat shock protein (Hsp)70 and Hsp90α assist in matrix metalloproteinase-2 activation and breast cancer cell migration and invasion, PLoS One, 6, e18848, 10.1371/journal.pone.0018848 · DOI
  27. Eustace, 2004, Functional proteomic screens reveal an essential extracellular role for hsp90 alpha in cancer cell invasiveness, Nat Cell Biol, 6, 507, 10.1038/ncb1131 · DOI
  28. Vartholomaiou, 2017, Cytosolic Hsp90α and its mitochondrial isoform Trap1 are differentially required in a breast cancer model, Oncotarget, 8, 17428, 10.18632/oncotarget.15659 · DOI
  29. Wang, 2009, The regulatory mechanism of Hsp90alpha secretion and its function in tumor malignancy, Proc Natl Acad Sci USA, 106, 21288, 10.1073/pnas.0908151106 · DOI
  30. Wang, 2016, Hsp90AB1 protein is overexpressed in non-small cell lung cancer tissues and associated with poor prognosis in lung adenocarcinoma patients, Zhongguo Fei Ai Za Zhi, 19, 64
  31. Morales, 2014, Immune chaperone gp96 drives the contributions of macrophages to inflammatory colon tumorigenesis, Cancer Res, 74, 446, 10.1158/0008-5472.CAN-13-1677 · DOI
  32. Meng, 2017, Hsp90β promoted endothelial cell-dependent tumor angiogenesis in hepatocellular carcinoma, Mol Cancer, 16, 72, 10.1186/s12943-017-0640-9 · DOI
  33. Sunil Kumar, 2018, The overexpression of Hsp90B1 is associated with tumorigenesis of canine mammary glands, Mol Cell Biochem, 440, 23, 10.1007/s11010-017-3152-4 · DOI
  34. Rachidi, 2015, Endoplasmic reticulum heat shock protein gp96 maintains liver homeostasis and promotes hepatocellular carcinogenesis, J Hepatol, 62, 879, 10.1016/j.jhep.2014.11.010 · DOI
  35. Yang, 2015, Upregulation of heat shock proteins (HSPA12A, HSP90B1, HSPA4, HSPA5 and HSPA6) in tumour tissues is associated with poor outcomes from HBV-related early-stage hepatocellular carcinoma, Int J Med Sci, 12, 256, 10.7150/ijms.10735 · DOI
  36. Hou, 2015, Plasma membrane gp96 enhances invasion and metastatic potential of liver cancer via regulation of uPAR, Mol Oncol, 9, 1312, 10.1016/j.molonc.2015.03.004 · DOI
  37. Chen, 2015, Expression of heat-shock protein gp96 in gallbladder cancer and its prognostic clinical significance, Int J Clin Exp Pathol, 8, 1946
  38. Xu, 2016, HSP90B1 overexpression predicts poor prognosis in NSCLC patients, Tumour Biol, 37, 14321, 10.1007/s13277-016-5304-7 · DOI
  39. Agorreta, 2014, TRAP1 regulates proliferation, mitochondrial function, and has prognostic significance in NSCLC, Mol Cancer Res, 12, 660, 10.1158/1541-7786.MCR-13-0481 · DOI
  40. Sisinni, 2017, TRAP1 controls cell cycle G2-M transition through the regulation of CDK1 and MAD2 expression/ubiquitination, J Pathol, 243, 123, 10.1002/path.4936 · DOI
  41. Schaal, 2014, Nicotine-mediated cell proliferation and tumor progression in smoking-related cancers, Mol Cancer Res, 12, 14, 10.1158/1541-7786.MCR-13-0541 · DOI
  42. Cardinale, 2012, Nicotine: Specific role in angiogenesis, proliferation and apoptosis, Crit Rev Toxicol, 42, 68, 10.3109/10408444.2011.623150 · DOI
  43. Wu, 2002, Involvement of human heat shock protein 90 alpha in nicotine-induced apoptosis, Int J Cancer, 100, 37, 10.1002/ijc.10449 · DOI
  44. Siegelin, 2013, Inhibition of the mitochondrial Hsp90 chaperone network: A novel, efficient treatment strategy for cancer?, Cancer Lett, 333, 133, 10.1016/j.canlet.2013.01.045 · DOI
  45. Singh, 2015, Topically applied Hsp90 inhibitor 17AAG inhibits UVR-induced cutaneous squamous cell carcinomas, J Invest Dermatol, 135, 1098, 10.1038/jid.2014.460 · DOI

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Metadata

Authors
Liu, K., Kang, M., Li, J., Qin, W., & Wang, R.
Affiliations
First Affiliated Hospital of GuangXi Medical University (CN)
Corresponding author
Wang, Rensheng
Venue
Experimental and Therapeutic Medicine
Published
2019-01-31
Volume
17
Issue
4
Pages
2657-2665
ISSN
  • 1792-0981 (ISSN-L)
  • 1792-1015
OpenAlex
W2913876929
Cited by
47
References
1
Citations by year
2026: 2 · 2025: 4 · 2024: 5 · 2023: 14 · 2022: 5 · 2021: 7 · 2020: 8 · 2019: 2
FWCI
1.61
Type
journal article
Language
en
Open access
Licence
cc-by-nc-nd
Locations
  • Experimental and Therapeutic Medicine (publishedVersion, cc-by-nc-nd)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
Funders
  • National Natural Science Foundation of China (81460460, 81360405, 81760542)
  • China Postdoctoral Science Foundation (2016M602918XB)
  • Science and Technology Department of Guangxi Zhuang Autonomous (2016GXNSFAA380252, 2014GXNSFBA118114)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heat shock proteins research
  • Health Sciences › Medicine › Oncology › Lung Cancer Research Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Breast Cancer Treatment Studies
Keywords
non-small cell lung cancer, HSP90AA1, HSP90AB1, HSP90B1, TRAP1, mRNA expression, prognostic factors, overall survival, adenocarcinoma, squamous cell carcinoma, therapeutic target

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