The Expression of Glypican-3 in Colorectal Cancer


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

Abstract—Glypican-3 (GPC3), a heparan sulfate proteoglycan is an emerging tumor marker; its overexpression has been stated in several types of cancer such as hepatocellular carcinoma (HCC), melanoma and etc. In this study, the expression of the GPC3 mRNA was investigated in 61 human colorectal cancer (CRC) tissues and 61 normal adjacent tissues, using the real-time PCR assay. Using immunohistochemistry (IHC), the expression of the GPC3 protein was examined in the cases that showed a marked elevation in the expression of the GPC3 mRNA in the tumor tissues, compared to the normal tissues. A significant increase in the expression of the GPC3 gene was revealed in 49.2% of the cases of CRC tumors, compared to the normal adjacent tissues. The expression of the GPC3 mRNA was found to significantly correlate with the pathological differentiation and the age of the patients. Interestingly, a significant reduction in the expression of the GPC3 mRNA was found in the tumor tissues of the 16 patients, who underwent the neoadjuvant chemotherapy, compared to the normal adjacent tissues. Unexpectedly, the GPC3 protein was not detected by IHC in 30 tissues, exhibiting the upregulation in the expression of the GPC3 mRNA. Our results indicated that GPC3 could be expressed in the CRC tissues at the mRNA level, while its expression could not be found at the protein level.

About the authors

Sonia Azizpour

Research Center for Molecular Medicine, Hamadan University of Medical Sciences

Email: aminra14@gmail.com
Iran, Islamic Republic of, Hamadan

Razieh Ezati

Institute of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology

Email: aminra14@gmail.com
Iran, Islamic Republic of, Tehran

Massoud Saidijam

Research Center for Molecular Medicine, Hamadan University of Medical Sciences

Email: aminra14@gmail.com
Iran, Islamic Republic of, Hamadan

Amirnader Emami Razavi

Cancer Biology Research Center, Cancer Institute of Iran, Tehran University of Medical Sciences

Author for correspondence.
Email: aminra14@gmail.com
Iran, Islamic Republic of, Tehran

Farid Azizi Jalilian

Microbiology Department, Faculty of Medicine, Hamadan University of Medical Sciences

Email: aminra14@gmail.com
Iran, Islamic Republic of, Hamadan

Ali Mahdavinezhad

Research Center for Molecular Medicine, Hamadan University of Medical Sciences

Email: aminra14@gmail.com
Iran, Islamic Republic of, Hamadan

Hamid Eslami

Research Center for Molecular Medicine, Hamadan University of Medical Sciences

Email: aminra14@gmail.com
Iran, Islamic Republic of, Hamadan

Alireza Soltanian

Modeling of Noncommunicable Disease Research Center, Department of Biostatistics, School of Public Health,
Hamadan University of Medical Sciences

Email: aminra14@gmail.com
Iran, Islamic Republic of, Hamadan

Hadiseh Mohammadpour

Cancer Research Center, Cancer Institute of Iran, Tehran university of Medical Sciences

Email: aminra14@gmail.com
Iran, Islamic Republic of, Tehran

Fatemeh Kamali

Cancer Biology Research Center, Cancer Institute of Iran, Tehran University of Medical Sciences

Email: aminra14@gmail.com
Iran, Islamic Republic of, Tehran

Razieh Amini

Research Center for Molecular Medicine, Hamadan University of Medical Sciences

Author for correspondence.
Email: aminra14@gmail.com
Iran, Islamic Republic of, Hamadan

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2019 Allerton Press, Inc.