Treatment-related survival associations of claudin-2 expression in fibroblasts of colorectal cancer.
Artur MezheyeuskiCarina StrellIna HrynchykTormod Kyrre GurenAnca DragomirTatyana DoroshenkoOksana PashkovaJulia GorgunKseniya RukshaPer PfeifferElin H KureHalfdan SorbyeDavid EdlerAnna MartlingBengt GlimeliusArne ÖstmanAnna PortyankoPublished in: Virchows Archiv : an international journal of pathology (2017)
Claudin-2 is a trans-membrane protein-component of tight junctions in epithelial cells. Elevated claudin-2 expression has been reported in colorectal cancer (CRC). The aim of this study was to investigate the expression patterns of claudin-2 in human CRC samples and analyze its association with clinical characteristics and treatment outcome. TMAs of primary tumors from two cohorts of metastatic CRC (mCRC) were used. Claudin-2 IHC staining was evaluated in a semi-quantitative manner in different regions and cell types. Claudin-2 expression was also analyzed by immunofluorescence in primary cultures of human CRC cancer-associated fibroblasts (CAFs). Initial analyses identified previously unrecognized expression patterns of claudin-2 in CAFs of human CRC. Claudin-2 expression in CAFs of the invasive margin was associated with shorter progression-free survival. Subgroup analyses demonstrated that the survival associations occurred among cases that received 5-FU+oxaliplatin combination treatment, but not in patients receiving 5-FU±irinotecan. The finding was validated by analyses of the independent cohort. In summary, previously unreported stromal expression of claudin-2 in CAFs of human CRC was detected together with significant association between high claudin-2 expression in CAFs and shorter survival in 5-FU+oxaliplatin-treated mCRC patients.
Keyphrases
- poor prognosis
- endothelial cells
- free survival
- binding protein
- long non coding rna
- end stage renal disease
- squamous cell carcinoma
- small cell lung cancer
- chronic kidney disease
- blood brain barrier
- clinical trial
- high resolution
- peritoneal dialysis
- single molecule
- drug induced
- extracellular matrix
- prognostic factors
- open label
- patient reported outcomes