Regulation of MDR1 expression and drug resistance by a positive feedback loop involving hyaluronan, phosphoinositide 3-kinase, and ErbB2

J Biol Chem. 2005 May 27;280(21):20310-5. doi: 10.1074/jbc.M500737200. Epub 2005 Mar 22.

Abstract

Multidrug resistance is a potent barrier to effective, long term therapy in cancer patients. It is frequently attributed to enhanced expression of multidrug transporters or to the action of receptor kinases, such as ErbB2, and downstream anti-apoptotic signaling pathways, such as the phosphoinositide 3-kinase/Akt pathway. However, very few connections have been made between receptor kinases or anti-apoptotic pathways and multidrug transporter expression or function. Data presented herein show that constitutive interaction of the pericellular polysaccharide, hyaluronan, with its receptor, CD44, regulates assembly and activation of an ErbB2-containing signaling complex, which in turn stimulates phosphoinositide 3-kinase activity in multidrug-resistant MCF-7/Adr human breast carcinoma cells. Phosphoinositide 3-kinase activates Akt and downstream anti-apoptotic events, which contribute to drug resistance. However, hyaluronan and phosphoinositide 3-kinase stimulate expression of the multidrug transporter, MDR1 (P-glycoprotein), in an interdependent, but Akt-independent, manner. Furthermore, constitutively active phosphoinositide 3-kinase, but not Akt, stimulates hyaluronan production. These Akt-independent effects are dominant over the effects of Akt on doxorubicin resistance in MCF-7/Adr cells. Thus hyaluronan, phosphoinositide 3-kinase, and ErbB2 form a positive feedback loop that strongly amplifies MDR1 expression and regulates drug resistance in these cells. This pathway may also be important in progression of other malignant characteristics. These results illustrate the potential importance of hyaluronan as a therapeutic target in multidrug-resistant carcinomas.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Breast Neoplasms
  • Brevican
  • Chondroitin Sulfate Proteoglycans / pharmacology
  • Doxorubicin
  • Drug Resistance, Neoplasm / genetics*
  • Feedback, Physiological
  • Gene Expression Regulation*
  • Genes, MDR / genetics*
  • Glucuronosyltransferase / genetics
  • Humans
  • Hyaluronan Receptors / genetics
  • Hyaluronan Receptors / pharmacology
  • Hyaluronan Receptors / physiology
  • Hyaluronan Synthases
  • Hyaluronic Acid / biosynthesis
  • Hyaluronic Acid / pharmacology
  • Hyaluronic Acid / physiology*
  • Lectins, C-Type
  • Nerve Tissue Proteins / pharmacology
  • Phosphatidylinositol 3-Kinases / physiology*
  • Phosphorylation
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / physiology
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / physiology
  • Proto-Oncogene Proteins c-akt
  • RNA, Small Interfering / pharmacology
  • Receptor, ErbB-2 / physiology*
  • Transfection
  • Tumor Cells, Cultured

Substances

  • BCAN protein, human
  • Brevican
  • Chondroitin Sulfate Proteoglycans
  • Hyaluronan Receptors
  • Lectins, C-Type
  • Nerve Tissue Proteins
  • Proto-Oncogene Proteins
  • RNA, Small Interfering
  • Doxorubicin
  • Hyaluronic Acid
  • Glucuronosyltransferase
  • Hyaluronan Synthases
  • Receptor, ErbB-2
  • AKT1 protein, human
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt