The efficacy of phloridzin and phloretin on tumor cell growth.

Abstract

This study utilized phloridzin (P1) and its aglucone phloretin (P2), two known inhibitors of glucose transmembrane transport, to inhibit tumor cell growth in vivo. The efficacy of hydrazine sulfate as an anticachexic agent was also evaluated. Utilizing the rat mammary adenocarcinoma and Fischer bladder cell carcinoma cell lines, it has been shown that the i.p. administration of P1 and P2 can produce significant differences in mean tumor diameters as compared to the untreated controls.

• Authors: J A Nelson, R E Falk
• Journal: Anticancer research (Anticancer Res) 1993 Nov-Dec Vol. 13 Issue 6A Pg. 2287-92 ISSN: 0250-7005 [Print] Greece
• PMID: 8297148 (Publication Type: Journal Article)

Chemical References

• Antineoplastic Agents
• Blood Glucose
• Phlorhizin
• Phloretin

Topics

• Adenocarcinoma (drug therapy, metabolism, pathology)
• Animals
• Antineoplastic Agents (therapeutic use, toxicity)
• Blood Glucose (drug effects, metabolism)
• Carcinoma, Transitional Cell (drug therapy, metabolism, pathology)
• Cell Division (drug effects)
• Female
• Glycosuria
• Male
• Mammary Neoplasms, Experimental (drug therapy, metabolism, pathology)
• Phloretin (therapeutic use, toxicity)
• Phlorhizin (therapeutic use, toxicity)
• Rats
• Rats, Inbred F344
• Time Factors
• Urinary Bladder Neoplasms (drug therapy, metabolism, pathology)