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GRP78 regulates CD44v membrane homeostasis and cell spreading in tamoxifen-resistant breast cancer.
Tseng, Chun-Chih; Stanciauskas, Ramunas; Zhang, Pu; Woo, Dennis; Wu, Kaijin; Kelly, Kevin; Gill, Parkash S; Yu, Min; Pinaud, Fabien; Lee, Amy S.
Affiliation
  • Tseng CC; Department of Biochemistry and Molecular Medicine, University of Southern California, Los Angeles, CA, USA.
  • Stanciauskas R; University of Southern California Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA, USA.
  • Zhang P; Department of Biological Sciences, University of Southern California, Los Angeles, CA, USA.
  • Woo D; Department of Molecular Microbiology and Immunology, University of Southern California, Los Angeles, CA, USA.
  • Wu K; University of Southern California Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA, USA.
  • Kelly K; University of Southern California Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA, USA.
  • Gill PS; Department of Stem Cell Biology and Regenerative Medicine, University of Southern California, Los Angeles, CA, USA.
  • Yu M; Department of Medicine/Division of Hematology, University of Southern California, Los Angeles, CA, USA.
  • Pinaud F; Department of Medicine/Division of Hematology, University of Southern California, Los Angeles, CA, USA.
  • Lee AS; University of Southern California Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA, USA.
Life Sci Alliance ; 2(4)2019 08.
Article in En | MEDLINE | ID: mdl-31416894
GRP78 conducts protein folding and quality control in the ER and shows elevated expression and cell surface translocation in advanced tumors. However, the underlying mechanisms enabling GRP78 to exert novel signaling functions at cell surface are just emerging. CD44 is a transmembrane protein and an important regulator of cancer metastasis, and isoform switch of CD44 through incorporating additional variable exons to the extracellular juxtamembrane region is frequently observed during cancer progression. Using super-resolution dual-color single-particle tracking, we report that GRP78 interacts with CD44v in plasma membrane nanodomains of breast cancer cells. We further show that targeting cell surface GRP78 by the antibodies can effectively reduce cell surface expression of CD44v and cell spreading of tamoxifen-resistant breast cancer cells. Our results uncover new functions of GRP78 as an interacting partner of CD44v and as a regulator of CD44v membrane homeostasis and cell spreading. This study also provides new insights into anti-CD44 therapy in tamoxifen-resistant breast cancer.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Drug Resistance, Neoplasm / Hyaluronan Receptors / Heat-Shock Proteins Limits: Female / Humans Language: En Journal: Life Sci Alliance Year: 2019 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Drug Resistance, Neoplasm / Hyaluronan Receptors / Heat-Shock Proteins Limits: Female / Humans Language: En Journal: Life Sci Alliance Year: 2019 Document type: Article Affiliation country: Country of publication: