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CUB Domain-containing Protein 1 (CDCP1) Is Down-regulated by Active Hexose-correlated Compound in Human Pancreatic Cancer Cells
- Source :
- Anticancer Research. 38:6107-6111
- Publication Year :
- 2018
- Publisher :
- Anticancer Research USA Inc., 2018.
-
Abstract
- BACKGROUND/AIM We have previously reported that treatment of pancreatic cancer cells with active hexose-correlated compound (AHCC), an extract of a basidiomycete mushroom, decreases the levels of tumor-associated proteins including heat-shock protein 27 (HSP27), heat shock factor 1 (HSF1) and sex-determining region Y-box 2 (SOX2). The transmembrane glycoprotein, CUB domain-containing protein 1 (CDCP1) has been reported to be up-regulated in various cancers, and be associated with invasion and metastasis. The aim of this study was to examine the effect of AHCC on the expression of CDCP1 in KLM1-R cells. MATERIALS AND METHODS Gemcitabine-resistant pancreatic cancer cells (KLM1-R) were treated with AHCC (10 mg/ml) for 48 h. Western blot analysis of cell extracts with anti-CDCP1 or anti-actin antibodies was performed to assess the expression of CDCP1. RESULTS Expression of CDCP1 was reduced by AHCC treatment of KLM1-R cells, whereas expression of actin was not affected. The ratio of intensities of CDCP1/actin in AHCC-treated KLM1-R cells was significantly suppressed (p
- Subjects :
- 0301 basic medicine
Cancer Research
Blotting, Western
Down-Regulation
Deoxycytidine
03 medical and health sciences
0302 clinical medicine
Hsp27
Western blot
Antigens, CD
Antigens, Neoplasm
Polysaccharides
Cell Line, Tumor
Pancreatic cancer
Active hexose correlated compound
medicine
Humans
HSF1
biology
medicine.diagnostic_test
Chemistry
General Medicine
CUB domain
medicine.disease
Gemcitabine
Molecular biology
Actins
Neoplasm Proteins
Pancreatic Neoplasms
030104 developmental biology
Oncology
Drug Resistance, Neoplasm
030220 oncology & carcinogenesis
biology.protein
CDCP1
Antibody
Cell Adhesion Molecules
Subjects
Details
- ISSN :
- 17917530 and 02507005
- Volume :
- 38
- Database :
- OpenAIRE
- Journal :
- Anticancer Research
- Accession number :
- edsair.doi.dedup.....9440ddca98d662fd977c7362402692ef
- Full Text :
- https://doi.org/10.21873/anticanres.12961