GRP78 induction in cancer: therapeutic and prognostic implications.
By Amy S. Lee. Cancer Research, 2007
826 citations recorded by the source corpus.
Subfields: Cell Biology, Epidemiology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/2097879f2c89d6fd38e9aefb2f924321b8f733b5
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Citations in the corpus
- MYB function in normal and cancer cells (2008, methodology): “and has recently been used as a receptor for the delivery of toxic peptides to cancer cell”
- Pathogenesis of mucormycosis. (2012, background): “GRP78 (also known as BiP/HSPA5) was discovered as a cellular protein induced by glucose starvation [47].”
- Cell death and endoplasmic reticulum stress: disease relevance and therapeutic opportunities (2008, background): “Indeed, various chemical inhibitor approaches to antagonizing the GRP78 protein have been preclinically investigated as possible cancer therapies (reviewed in Ref”
- The impact of the unfolded protein response on human disease (2012, background): “Increased expression of BiP/GRP78, which is primarily regulated by ATF6, correlates with chemotherapeutic resistance and is observed in aggressive cancers (Lee, 2007).”
- ER chaperones in mammalian development and human diseases (2007, background): “in normal organs has prompted new directions in targeting cytotoxic agents into cancer cells [71,74,90].”