TY - JOUR
T1 - Monounsaturated and Diunsaturated Fatty Acids Sensitize Cervical Cancer to Radiation Therapy
AU - Muhammad, Naoshad
AU - Ruiz, Fiona
AU - Stanley, Jennifer
AU - Rashmi, Ramachandran
AU - Cho, Kevin
AU - Jayachandran, Kay
AU - Zahner, Michael C.
AU - Huang, Yi
AU - Zhang, Jin
AU - Markovina, Stephanie
AU - Patti, Gary J.
AU - Schwarz, Julie K.
N1 - Publisher Copyright:
© 2022 American Association for Cancer Research.
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Obesity induces numerous physiological changes that can impact cancer risk and patient response to therapy. Obese patients with cervical cancer have been reported to have superior outcomes following chemoradiotherapy, suggesting that free fatty acids (FFA) might enhance response to radiotherapy. Here, using preclinical models, we show that monounsaturated and diunsaturated FFAs (uFFA) radiosensitize cervical cancer through a novel p53-dependent mechanism. UFFAs signaled through PPARγ and p53 to promote lipid uptake, storage, and metabolism after radiotherapy. Stable isotope labeling confirmed that cervical cancer cells increase both catabolic and anabolic oleate metabolism in response to radiotherapy, with associated increases in dependence onmitochondrial fatty acid oxidation for survival. In vivo, supplementation with exogenous oleate suppressed tumor growth in xenografts after radiotherapy, an effect that could be partially mimicked in tumors from high fat diet-induced obese mice. These results suggest that supplementation with uFFAs may improve tumor responses to radiotherapy, particularly inp53wild-type tumors.
AB - Obesity induces numerous physiological changes that can impact cancer risk and patient response to therapy. Obese patients with cervical cancer have been reported to have superior outcomes following chemoradiotherapy, suggesting that free fatty acids (FFA) might enhance response to radiotherapy. Here, using preclinical models, we show that monounsaturated and diunsaturated FFAs (uFFA) radiosensitize cervical cancer through a novel p53-dependent mechanism. UFFAs signaled through PPARγ and p53 to promote lipid uptake, storage, and metabolism after radiotherapy. Stable isotope labeling confirmed that cervical cancer cells increase both catabolic and anabolic oleate metabolism in response to radiotherapy, with associated increases in dependence onmitochondrial fatty acid oxidation for survival. In vivo, supplementation with exogenous oleate suppressed tumor growth in xenografts after radiotherapy, an effect that could be partially mimicked in tumors from high fat diet-induced obese mice. These results suggest that supplementation with uFFAs may improve tumor responses to radiotherapy, particularly inp53wild-type tumors.
UR - http://www.scopus.com/inward/record.url?scp=85151771675&partnerID=8YFLogxK
U2 - 10.1158/0008-5472.CAN-21-4369
DO - 10.1158/0008-5472.CAN-21-4369
M3 - Article
C2 - 36214635
AN - SCOPUS:85151771675
SN - 0008-5472
VL - 82
SP - 4515
EP - 4527
JO - Cancer research
JF - Cancer research
IS - 24
ER -