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Clinicopathologic Significance of Heat Shock Protein 60 as a Survival Predictor in Colorectal Canceropen access

Authors
Kang, MyungheeJeong, SoyeonAn, JungsukPark, SungjinNam, SeungyoonKwon, Kwang AnSahoo, DebashisGhosh, PradiptaKim, Jung Ho
Issue Date
Aug-2023
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
colorectal cancer; heat shock protein 60; heat shock protein family D (HSP60) member 1; TNM classification
Citation
Cancers, v.15, no.16
Indexed
SCIE
SCOPUS
Journal Title
Cancers
Volume
15
Number
16
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/64030
DOI
10.3390/cancers15164052
ISSN
2072-6694
2072-6694
Abstract
The role of heat shock protein 60 (HSP60), a mitochondrial chaperone, in tumor progression or its anti-tumor effects remains controversial. This study aimed to confirm the possibility of using HSP60 as a prognostic marker in patients with colorectal cancer (CRC), considering TNM classification for precise prediction. HSP60 expression increased with differentiation and p53 mutations in patients. However, compared to patients with high HSP60 expression, patients with low HSP60 expression had event-free survival and disease-specific survival hazard ratios (HRs) of 1.42 and 1.69, respectively. Moreover, when the survival rate was analyzed by combining TNM classification and HSP60 expression, the prognosis was poor, particularly when HSP60 expression was low in the late/advanced stage. This pattern was also observed with HSP family D member 1, HSPD1, the gene that encodes HSP60. Low HSPD1 expression was linked to lower overall survival and relapse-free survival rates, with HRs of 1.80 and 1.87, respectively. When TNM classification and HSPD1 expression were considered, CRC patients with low HSPD1 expression and advanced malignancy had a poorer prognosis than those with high HSPD1 expression. Thus, HSPD1/HSP60 can be a useful biomarker for a sophisticated survival prediction in late- and advanced-stage CRC, allowing the design of individualized treatment strategies.
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2. Clinical Science > Department of Pathology > 1. Journal Articles
4. Research institute > Institute of Convergence New Drug Development > 1. Journal Articles

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