mProX™ Human ERBB2 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 Overexpression of ERBB2 promotes autophagy in breast cancer cells.
The overexpression of ERBB2 resulted in a minimum 40% increase in basal and amino acid starvation-induced levels of autophagy, as determined by LC3-II Western blotting, in the breast cancer cell lines MDA-MB-231 (ERBB2-negative) and MCF 7 (ERBB2-positive).
Ref: Chen, Yongqiang, et al. "Erb-b2 receptor tyrosine kinase 2 (ERBB2) promotes ATG12-dependent autophagy contributing to treatment resistance of breast cancer cells." Cancers 13.5 (2021): 1038.
Pubmed: 33801244
DOI: 10.3390/cancers13051038
Research Highlights
The scoring accuracy for ERBB2 IHC in the low range was subpar in this investigation utilizing the current standard ERBB2 IHC assay. In the actual world, this error could misidentify a large number of patients for T-DXd treatment.
Fernandez, Aileen I., et al. "Examination of low ERBB2 protein expression in breast cancer tissue." JAMA oncology 8.4 (2022): 1-4.
Pubmed:
35113160
DOI:
10.1001/jamaoncol.2021.7239
ErbB2 (or HER-2) is at the nexus of cancer and chronic heart failure due to its dual roles in tumor growth and the heart's physiological adaptive responses. Thus, activation of ErbB2 for heart failure therapy may induce malignancy, and ErbB2-targeted inhibitory therapy for cancer may cause ventricular dysfunction.
Vermeulen, Zarha, Vincent FM Segers, and Gilles W. De Keulenaer. "ErbB2 signaling at the crossing between heart failure and cancer." Basic research in cardiology 111 (2016): 1-14.
Pubmed:
27596216
DOI:
10.1007/s00395-016-0576-z