Receptors for Targeting Gastrointestinal Tract Cancer
AAPS Advances in the Pharmaceutical Sciences Series, ISSN: 2210-738X, Vol: 39, Page: 141-170
2019
- 1Citations
- 4Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Book Chapter Description
Cancers of the gastrointestinal tract (GIT)Gastrointestinal tract (GIT) are among the most prevalent and fatal cancers. Historically, surgical resection was the only effective treatment of operable GIT tumors. However, more than half of these patients present locally advanced, recurrent, or metastatic disease, necessitating development of alternate strategies for possible therapy. Cellular receptors are instrumental in controlling the basic traits of a cell. Binding of specific ligands to these receptors results in changes in gene expression and increase in cell metabolism, cell growth, or cell death. The therapeutic prospects of ligands for somatostatin receptors (SSTRs), c-Kit, and peroxisome proliferator-activated receptors (PPARs) along with receptor-mediated strategies have been discussed in this chapter. Ligands for these receptors include peptides, small molecules, and oligonucleotides that can be delivered using nanoparticulate delivery systems tailored for specific application. Some important drug candidates undergoing clinical trials have also been mentioned to convey the potential of these receptors as targets for GIT cancer therapy.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85081149781&origin=inward; http://dx.doi.org/10.1007/978-3-030-29168-6_5; http://link.springer.com/10.1007/978-3-030-29168-6_5; https://dx.doi.org/10.1007/978-3-030-29168-6_5; https://link.springer.com/chapter/10.1007/978-3-030-29168-6_5
Springer Science and Business Media LLC
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