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

Author:

Kang Myunghee1ORCID,Jeong Soyeon2ORCID,An Jungsuk3ORCID,Park Sungjin4,Nam Seungyoon45,Kwon Kwang An6,Sahoo Debashis78,Ghosh Pradipta91011,Kim Jung Ho26ORCID

Affiliation:

1. Department of Pathology, Gachon University Gil Medical Center, College of Medicine, Gachon University, Incheon 21565, Republic of Korea

2. Gachon Medical Research Institute, Gachon Biomedical Convergence Institute, Gachon University Gil Medical Center, College of Medicine, Gachon University, Incheon 21565, Republic of Korea

3. Department of Pathology, Korea University Anam Hospital, College of Medicine, Korea University, Seoul 02841, Republic of Korea

4. Department of Genome Medicine and Science, AI Convergence Center for Medical Science, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon 21565, Republic of Korea

5. Department of Health Sciences and Technology, Gachon Advanced Institute for Health Sciences and Technology (GAIHST), Gachon University, Incheon 21565, Republic of Korea

6. Department of Internal Medicine, Gachon University Gil Medical Center, College of Medicine, Gachon University, Incheon 21565, Republic of Korea

7. Department of Computer Science and Engineering, University of California, San Diego, CA 92093, USA

8. Department of Pediatrics, University of California, San Diego, CA 92093, USA

9. Department of Cellular and Molecular Medicine, University of California, San Diego, CA 92093, USA

10. Department of Medicine, University of California, San Diego, CA 92093, USA

11. HUMANOID Center of Research Excellence (CoRE), University of California, San Diego, CA 92093, USA

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.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

Reference41 articles.

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