Tegillarca granosa extract Haishengsu (HSS) suppresses expression of mdr1, BCR/ABL and sorcin in drug-resistant K562/ADM tumors in mice

Adv Med Sci. 2013;58(1):112-7. doi: 10.2478/v10039-012-0069-8.

Abstract

Purpose: To evaluate the effect of Haishengsu (HSS), a protein extract from Tegillarca granosa, on multidrug-resistance genes mdr1, BCR/ABL and sorcin in transplanted tumors.

Material/methods: Mice were inoculated subcutaneously with a drug resistant leukemia cell line K562/ADM. Tumor-bearing animals were divided into control, adriamycin, HSS and combination therapy (adriamycin plus HSS) groups. Flow cytometry was used to detect apoptosis of tumor cells, and RT-PCR was used to evaluate the expression of mdr1, BCR/ABL and sorcin.

Results: The apoptosis rate in the high (71.8%), medium (72.3%) and low doses HSS group (72.4%) was higher than in control (1.2%, p<0.01), adriamycin (34.4%, p<0.05) or combination therapy group (46.4%, p<0.05). The mean optical density of mdr1, BCR/ABL and sorcin in HSS groups was lower than in control, adriamycin and combination therapy group (p<0.01). The optical density of the three genes in high HSS group was lower than in medium and low HSS group (p<0.01).

Conclusions: Haishengsu promotes apoptosis of drug-resistant K562/ADM tumors in mice in a dose-dependent manner. The pro-apoptotic effect of Haishengsu may be related to a reduced expression of multidrug-resistance genes mdr1, BCR/ABL and sorcin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism*
  • Albumins / pharmacology*
  • Animals
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology
  • Apoptosis
  • Bivalvia / metabolism
  • Calcium-Binding Proteins / metabolism*
  • Caspase 3 / metabolism
  • Dose-Response Relationship, Drug
  • Doxorubicin / pharmacology
  • Drug Resistance, Multiple
  • Drug Resistance, Neoplasm*
  • Drugs, Chinese Herbal / pharmacology*
  • Female
  • Flow Cytometry
  • Fusion Proteins, bcr-abl / metabolism*
  • Gene Expression Profiling
  • Humans
  • K562 Cells
  • Mice
  • Mice, Nude
  • Neoplasm Transplantation

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Albumins
  • Calcium-Binding Proteins
  • Drugs, Chinese Herbal
  • SRI protein, human
  • haishengsu
  • Doxorubicin
  • Fusion Proteins, bcr-abl
  • Caspase 3