New study sheds light to colorectal cancer recurrence
New study sheds light to colorectal cancer recurrence16 Nov 2015
Cetuximab, marketed as Erbitux®, is one of the key therapies for metastatic colorectal cancer. Yet the cancer still returns in some patients, shortening overall survival.
A study at The University of Texas MD Anderson Cancer Center may help explain why the body sometimes becomes resistant to this therapy. The results reveal new insight into how key proteins, known as epidermal growth factor receptors (EGFR), are regulated, leading to resistance.
Why does the body become resistant to cetuximab treatment?
Methylation is a process by which proteins are chemically altered. EGFR, when expressed aberrantly, can lead to cellular changes including runaway cell growth, reduced cell death, tumor formation and metastasis. Mien Chie Hung, Ph.D., chair of Molecular and Cellular Oncology and colleagues found that expression of methylation-defective EGFR reduced tumor growth in mice.
“More importantly, we showed that increased methylation of EGFR resulted in resistance to cetuximab mediated cancer cell growth,” said Hung. “This correlated with poorer clinical outcomes observed in colorectal cancer patients and higher recurrence rates following cetuximab treatment.”
How methylation is linked with resistance to cetuximab treatment?
The study showed that EGFR methylation was mediated by PRMT1, a protein involved in a variety of genetic processes including gene transcription, DNA repair and signaling.
“EGFR methylation sustained signaling activity and cell proliferation even in the presence of cetuximab,” said Hung. “This data suggests that this specific methylation plays an important role in regulating EGFR functionality and resistance to cetuximab treatment.”Source: MD Anderson Cancer Center