Elucidating the role of enzyme MAPK6 in cancer has been quite a challenge.
“Some studies concluded that MAPK6 promoted cancer growth while others indicated the opposite effect,” said corresponding author Dr. Feng Yang, assistant professor of molecular and cellular biology at Baylor. “In the current study, we investigated the role of MAPK6 in several cancer cell lines and animal models of the condition and also the mechanism mediating its effects.”
Yang and his colleagues began by investigating the effect of overexpressing the MAPK6 gene in normal human prostate or breast epithelial cells grown in the lab.
“We found that overexpressing MAPK6 can transform normal cells into tumor-like cells,” said Yang, a member of Baylor’s Dan L Duncan Comprehensive Cancer Center. “In addition, enhancing MAPK6 expression in prostate, ovarian, breast and non-small cell lung cancer cell lines that already had low to high levels of MAPK6 further promoted growth of all tumor cell lines.”
These findings suggested that eliminating MAPK6 from tumor cells could reduce tumor growth. Indeed, genetically knocking down MAPK6 significantly reduced the growth of several types of cancer cells in the lab.
Understanding how MAPK6 promotes cancer growth suggests a potential therapeutic strategy
The researchers then investigated the mechanism mediating MAPK6 cancer-promoting activity.
“We had previously found that MAPK4, which is closely related to MAPK6, promotes cancer growth by activating the AKT pathway,” Yang said.
Here, we discovered that MAPK6 also activates AKT to promote cancer growth.”
“Both MAPK4 and MAPK6 add a phosphate group to AKT, a process called phosphorylation, but MAPK6 phosphorylates a different location in AKT than does MAPK4, and this is essential for the tumor-promoting activity of MAPK6.”
MAPK6 adds a phosphate group to AKT location identified as S473, which is the same location that is phosphorylated by a cancer-promoting mTOR protein kinase complex called mTORC2.
“MAPK6 appears to phosphorylate location S473 in AKT independently of mTORC2,” Yang said. “This is important because it may have relevant clinical implications.”
Kinase inhibitors for mTOR are currently being tested in clinical trials for their ability to reduce cancer growth; however, over time cancer cells seem to resist this inhibitory effect and continue to grow. Yang and colleagues’ findings in the lab show that while inhibiting MAPK6 and mTOR activities separately reduces AKT phosphorylation and cancer cell growth, inhibiting both simultaneously achieves a more robust tumor-suppressing activity.
Our findings show that the cancer-promoting pathway AKT can be activated independently by mTORC2 and MAPK6.”
“Therefore, we propose that inhibiting mTORC2 activity does not effectively control cancer growth because, in many cases, MAPK6 may compensate for the lack of mTORC2 activity by independently sustaining AKT activation and cancer growth,” Yang explained.
The findings suggest that MAPK6 provides cancer cells with a way to escape the growth-suppressing effect of mTOR inhibitors that has been observed in the clinic.
“More studies are needed, but we suggest that combining both MAPK6 and mTOR inhibitors might provide a more effective and longer-lasting approach to reduce cancer growth,” Yang said.
Learn all the details of this study in the journal Science Advances.
Other contributors to this work include Qinbo Cai, Wolong Zhou, Wei Wang, Bingning Dong, Dong Han, Tao Shen, Chad J. Creighton and David D. Moore. The authors are affiliated with one or more of the following institutions: Baylor College of Medicine, First Affiliated Hospital of Sun Yat-sen University, Xiangya Hospital of Central South University and University of California – Berkeley.
This research was supported by grants from the Department of Defense Congressionally Directed Medical Research Programs (W81XWH-17-1-0043), the Cancer Prevention and Research Institute of Texas (RP130651) and the National Institutes of Health (CA125123).
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