Abstract
Pancreatic cancer has proven to be one of the most difficult diseases to detect, diagnose, and treat due to both the location of the pancreas in the abdomen and the lack of overt symptoms before cancer dissemination. Thus, it is critical to have a variety of modeling systems that can be employed to evaluate drug responses/mechanisms while providing a relatively simple format for drug screening. Cell culture serves this purpose. In this context, it is necessary to review the available pancreatic cancer cell lines, culture techniques, predominant signaling pathways, and types of analyses that can be utilized to assess the effectiveness of drugs on pancreatic cancer cells, including aspects of pharmocotherapeutic strategies for the development of novel methodologies. Special consideration will be given to different signal transduction pathways like MAPK, JAK/STAT, PI3K/AKT, RTKs, VEGF, and NF-κB, which are involved in various aspects of pancreatic cancer development and progression, complete with a repertoire of chemical inhibition at several levels within a cascade. Ultimately, abrogation of these cell signals can be detected through measurable variables at the cellular level, including apoptosis, proliferation, altered cell phenotype, the ability to invade and/or metastasize, and changes in cell cycle parameters. Evaluation of drugs at this level can set the stage for future strategies as well as exploration of novel compounds that inhibit other vital cancer signaling pathways.
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Mullapudi, B., Ding, Y., Ding, X., Grippo, P. (2010). Drug Evaluations in Pancreatic Cancer Culture Systems. In: Han, H., Grippo, P. (eds) Drug Discovery in Pancreatic Cancer. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-1160-5_1
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