Pancreatic ductal adenocarcinoma(PDAC)is the third leading cause of cancerrelated deaths in the United States.Although chemotherapeutic regimens such as gemcitabine+nab-paclitaxel and FOLFIRINOX(FOLinic acid,5-Fluroru...Pancreatic ductal adenocarcinoma(PDAC)is the third leading cause of cancerrelated deaths in the United States.Although chemotherapeutic regimens such as gemcitabine+nab-paclitaxel and FOLFIRINOX(FOLinic acid,5-Fluroruracil,IRINotecan,and Oxaliplatin)significantly improve patient survival,the prevalence of therapy resistance remains a major roadblock in the success of these agents.This review discusses the molecular mechanisms that play a crucial role in PDAC therapy resistance and how a better understanding of these mechanisms has shaped clinical trials for pancreatic cancer chemotherapy.Specifically,we have discussed the metabolic alterations and DNA repair mechanisms observed in PDAC and current approaches in targeting these mechanisms.Our discussion also includes the lessons learned following the failure of immunotherapy in PDAC and current approaches underway to improve tumor’s immunological response.展开更多
文摘Pancreatic ductal adenocarcinoma(PDAC)is the third leading cause of cancerrelated deaths in the United States.Although chemotherapeutic regimens such as gemcitabine+nab-paclitaxel and FOLFIRINOX(FOLinic acid,5-Fluroruracil,IRINotecan,and Oxaliplatin)significantly improve patient survival,the prevalence of therapy resistance remains a major roadblock in the success of these agents.This review discusses the molecular mechanisms that play a crucial role in PDAC therapy resistance and how a better understanding of these mechanisms has shaped clinical trials for pancreatic cancer chemotherapy.Specifically,we have discussed the metabolic alterations and DNA repair mechanisms observed in PDAC and current approaches in targeting these mechanisms.Our discussion also includes the lessons learned following the failure of immunotherapy in PDAC and current approaches underway to improve tumor’s immunological response.
