1993Journal of Gastroenterology and HepatologyRequires access

Expression of multidrug resistance (P‐glycoprotein) gene in liver cancers

M. Tien Kuo, Larry D. Teeter, Steven A. Curley, H C Hsu

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Abstract

Abstract Hepatocellular carcinomas have been known to exhibit a poor response to chemotherapeutic agents. However, the mechanism for drug resistance is unknown. Recent studies have demonstrated that expression of a group of membrane proteins known as P‐glycoproteins (P‐gp) or multidrug transporters encoded by multidrug‐resistance (MDR) or P‐glycoprotein gene family is correlated with a poor clinical prognosis for particular non‐responsive neoplasms. The possible involvement ofMDRgene expression with the intrinsic poor response to chemotherapeutic agents is discussed.

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What this paper is about

Abstract Hepatocellular carcinomas have been known to exhibit a poor response to chemotherapeutic agents. However, the mechanism for drug resistance is unknown. Recent studies have demonstrated that expression of a group of membrane proteins known as P‐glycoproteins (P‐gp) or multidrug transporters encoded by multidrug‐resistance (MDR) or P‐glycoprotein gene family is correlated with a poor clinical prognosis for particular non‐responsive neoplasms. The possible involvement ofMDRgene expression with the intrinsic poor response to chemotherapeutic agents is discussed.

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Available abstract

Abstract Hepatocellular carcinomas have been known to exhibit a poor response to chemotherapeutic agents. However, the mechanism for drug resistance is unknown. Recent studies have demonstrated that expression of a group of membrane proteins known as P‐glycoproteins (P‐gp) or multidrug transporters encoded by multidrug‐resistance (MDR) or P‐glycoprotein gene family is correlated with a poor clinical prognosis for particular non‐responsive neoplasms. The possible involvement ofMDRgene expression with the intrinsic poor response to chemotherapeutic agents is discussed.

Key concepts: Multiple drug resistance, P-glycoprotein, Medicine, Gene, Drug resistance, Gene expression, Glycoprotein, Transporter

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