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Differences in the immunosurveillance pattern associated with DNA mismatch repair status between right‐sided and left‐sided colorectal cancer
- Source :
- Cancer Science
- Publication Year :
- 2020
- Publisher :
- Wiley, 2020.
-
Abstract
- Tumor location and immunity play important roles in the progression of colorectal cancer (CRC). This study aimed to investigate the differences in the immunosurveillance pattern between right‐ and left‐sided CRC and analyze their association with clinicopathologic features, including mismatch repair (MMR) status. We included surgically resected stage II/III CRC cases and evaluated the immunohistochemical findings of HLA class I, HLA class II, programmed cell death‐ligand 1 (PD‐L1), PD‐1, CTLA‐4, CD3, CD4, CD8, TIA‐1, T‐bet, GATA3, RORγT, Foxp3, and CD163. A total of 117 patients were included in the analyses; of these, 30 and 87 had right‐ and left‐sided cancer, respectively. Tumor immunity varied according to the tumor location in the overall cohort. Analysis of the tumors excluding those with DNA mismatch repair (MMR) deficiency also revealed that tumor immunity differed according to the tumor location. In right‐sided colon cancer (CC), high expression of Foxp3 (P = .0055) and TIA‐1 (P = .0396) were associated with significantly better disease‐free survival (DFS). High CD8 (P = .0808) and CD3 (P = .0863) expression tended to have better DFS. Furthermore, in left‐sided CRC, only high PD‐L1 expression in the stroma (P = .0426) was associated with better DFS. In multivariate analysis, high Foxp3 expression in right‐sided CC was an independent prognostic factor for DFS (hazard ratio, 7.6445; 95% confidence interval, 1.2091‐150.35; P = .0284). In conclusion, the immunosurveillance pattern differs between right‐ and left‐sided CRC, even after adjusting for MMR deficiency.<br />Comparison of Kaplan‐Meier curves of disease‐free survival (DFS) in each tumor location excluding DNA mismatch repair deficiency. In right‐sided colon cancer, high Foxp3 (P = .0055) and TIA‐1 expression (P = .0396) were associated with significantly better DFS. High CD8 (P = .0808) and CD3 (0.0863) expression showed a tendency towards better DFS. In left‐sided colorectal cancer, only high sPD‐L1 expression (P = .0426) was associated with better DFS.
- Subjects :
- Male
0301 basic medicine
Oncology
Cancer Research
CD3 Complex
Colorectal cancer
tumor‐infiltrating lymphocyte
DNA Mismatch Repair
B7-H1 Antigen
0302 clinical medicine
Pathology
Immunologic Surveillance
Aged, 80 and over
Hazard ratio
FOXP3
Forkhead Transcription Factors
General Medicine
Middle Aged
Immunosurveillance
mismatch repair
030220 oncology & carcinogenesis
Original Article
Female
DNA mismatch repair
Colorectal Neoplasms
immune‐checkpoint molecule
Adult
medicine.medical_specialty
Colon
CD8 Antigens
colorectal cancer
Human leukocyte antigen
Disease-Free Survival
03 medical and health sciences
Internal medicine
Biomarkers, Tumor
medicine
Humans
tumor location
Aged
business.industry
Tumor-infiltrating lymphocytes
Rectum
Cancer
Original Articles
medicine.disease
T-Cell Intracellular Antigen-1
030104 developmental biology
business
Subjects
Details
- ISSN :
- 13497006 and 13479032
- Volume :
- 111
- Database :
- OpenAIRE
- Journal :
- Cancer Science
- Accession number :
- edsair.doi.dedup.....445fd9c37d47148f368d2f9c9d99dbba