This article is
- freely available
Novel Molecular Targets for the Treatment of Gastroenteropancreatic Endocrine Tumors: Answers and Unsolved Problems
Digestive and Liver Disease Unit, S. Andrea Hospital, Faculty of Medicine and Psychology, Sapienza University of Rome at S. Andrea Hospital, Via di Grottarossa 1035, 00189 Rome, Italy
Department of Surgery, Philipps-University, Marburg, Germany
* Author to whom correspondence should be addressed.
Received: 11 October 2012; in revised form: 1 December 2012 / Accepted: 3 December 2012 / Published: 20 December 2012
Abstract: As more knowledge on molecular alterations favoring carcinogenesis and spreading of gastroenteropancreatic endocrine tumors has become available, a number of targeted agents interfering with key growth and angiogenic pathways have been explored in preclinical and clinical studies. The mTOR inhibitor Everolimus, and the multi-target antiangiogenetic agent Sunitinib, have been shown to be effective and thus have been approved by the FDA for treatment of pancreatic endocrine tumors. However, there is little data on the primary resistance to targeted agents on these tumors. The goals of the present review are to elucidate the possible advantage of combined treatments in overcoming induced resistances, and to identify biomarkers able to predict clinical efficacy. Moreover, the role of interesting targets for which a strong biological rationale exists, and specific inhibitors are available, such as the Src Family Kinases and the Hedgehog Pathway, are discussed. There is now need for more preclinical studies on cell lines and animal models to provide a stronger preclinical background in this field, as well as clinical trials specifically comparing one targeted therapy with another or combining different targeted agents.
Keywords: gastroenteropancreatic endocrine tumors; target therapy; mTOR; angiogenesis; Src; hedgehog; combined treatment; resistance
Article StatisticsClick here to load and display the download statistics.
Notes: Multiple requests from the same IP address are counted as one view.
Cite This Article
MDPI and ACS Style
Capurso, G.; Fendrich, V.; Rinzivillo, M.; Panzuto, F.; Bartsch, D.K.; Fave, G.D. Novel Molecular Targets for the Treatment of Gastroenteropancreatic Endocrine Tumors: Answers and Unsolved Problems. Int. J. Mol. Sci. 2013, 14, 30-45.
Capurso G, Fendrich V, Rinzivillo M, Panzuto F, Bartsch DK, Fave GD. Novel Molecular Targets for the Treatment of Gastroenteropancreatic Endocrine Tumors: Answers and Unsolved Problems. International Journal of Molecular Sciences. 2013; 14(1):30-45.
Capurso, Gabriele; Fendrich, Volker; Rinzivillo, Maria; Panzuto, Francesco; Bartsch, Detlef K.; Fave, Gianfranco D. 2013. "Novel Molecular Targets for the Treatment of Gastroenteropancreatic Endocrine Tumors: Answers and Unsolved Problems." Int. J. Mol. Sci. 14, no. 1: 30-45.