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Galectin-9 expression as a poor prognostic factor in patients with renal cell carcinoma
- Source :
- Cancer Immunology, Immunotherapy. 69:2041-2051
- Publication Year :
- 2020
- Publisher :
- Springer Science and Business Media LLC, 2020.
-
Abstract
- Recently, the effectiveness of anti-programmed death 1 (PD-1) antibody therapy in the treatment of renal cell carcinoma (RCC) has been established. Nevertheless, efficacy has been reported to be limited to only 10–30% of patients. To develop more effective immunotherapy for RCC, we analyzed the immunological characteristics in RCC tissues by immunohistochemistry (IHC). We prepared a tissue microarray that consisted of tumor tissue sections (1 mm in diameter) from 83 RCC patients in Kanagawa Cancer Center between 2006 and 2015. IHC analysis was performed with antibodies specific to immune-related (CD8 and Foxp3) and immune checkpoint (programmed death ligand 1 (PD-L1) and 2 (PD-L2), B7-H4 and galectin-9) molecules. The numbers and proportions of positively stained tumor cells or immune cells were determined in each section. From multivariate analysis of all 83 patients, higher galectin-9 expression was detected as a factor associated with worse overall survival (OS) (P = 0.029) and that higher stage and higher B7-H4 expression were associated with worse progression-free survival (PFS) (P
- Subjects :
- Adult
Male
Oncology
Cancer Research
medicine.medical_specialty
Galectins
medicine.medical_treatment
Immunology
03 medical and health sciences
0302 clinical medicine
Renal cell carcinoma
Internal medicine
Biomarkers, Tumor
medicine
Humans
Immunology and Allergy
Carcinoma, Renal Cell
Aged
Retrospective Studies
Aged, 80 and over
Tissue microarray
business.industry
FOXP3
Cancer
Immunotherapy
Middle Aged
Prognosis
medicine.disease
Kidney Neoplasms
Immune checkpoint
Survival Rate
Immunohistochemistry
Female
business
Clear cell
Follow-Up Studies
030215 immunology
Subjects
Details
- ISSN :
- 14320851 and 03407004
- Volume :
- 69
- Database :
- OpenAIRE
- Journal :
- Cancer Immunology, Immunotherapy
- Accession number :
- edsair.doi.dedup.....3c002afd68d37a3c4cfa46677d06a7fb
- Full Text :
- https://doi.org/10.1007/s00262-020-02608-6