Cbl-b regulates the sensitivity of cetuximab through ubiquitin-proteasome system in human gastric cancer cells.

Abstract

PURPOSE:

Cetuximab is a monoclonal antibody against epidermal growth factor receptor (EGFR) and is approved for clinical use in combination with chemotherapy in patients affected by colorectal cancer (CRC), non small cell lung cancer (NSCLC), and head and neck cancer. Compared with these cancers, gastric cancer is relatively resistant to cetuximab and its regulatory mechanism is still unclear.

METHODS:

In this study, we assessed whether the ubiquitin- proteasome pathway is involved in regulating cetuximab-induced cells apoptosis in MGC803 and BGC823 gastric cancer cell lines.

RESULTS:

The casitas B lineage lymphoma-b (Cbl-b), a kind of E3 ubiquitin ligase, was involved in this process. Specific silenced Cbl-b expression increased the expression of EGFR.

CONCLUSIONS:

Our findings lead to a better understanding of the mechanism of cetuximab action, and suggests that Cbl-b increases the sensitivity of cetuximab in gastric cancer cells.

• Authors: Ping Yu, Yibo Fan, Xiujuan Qu, Jingdong Zhang, Na Song, Jing Liu, Yunpeng Liu
• Journal: Journal of B.U.ON. : official journal of the Balkan Union of Oncology (J BUON) 2016 Jul-Aug Vol. 21 Issue 4 Pg. 867-873 ISSN: 1107-0625 [Print] Cyprus
• PMID: 27685907 (Publication Type: Journal Article)

Chemical References

• Adaptor Proteins, Signal Transducing
• Antibodies, Monoclonal
• Antineoplastic Agents
• Ubiquitin
• CBLB protein, human
• Proto-Oncogene Proteins c-cbl
• EGFR protein, human
• ErbB Receptors
• Proteasome Endopeptidase Complex
• Cetuximab

Topics

• Adaptor Proteins, Signal Transducing (metabolism)
• Antibodies, Monoclonal (pharmacology)
• Antineoplastic Agents (pharmacology)
• Apoptosis (drug effects)
• Cell Line, Tumor
• Cetuximab (pharmacology)
• Drug Resistance, Neoplasm (physiology)
• ErbB Receptors (metabolism)
• Humans
• Proteasome Endopeptidase Complex (metabolism)
• Proto-Oncogene Proteins c-cbl (metabolism)
• Stomach Neoplasms (drug therapy, metabolism)
• Ubiquitin (metabolism)