Reprint

Cancer Prevention with Molecular Target Therapies

Edited by
June 2023
208 pages
  • ISBN978-3-0365-7927-6 (Hardback)
  • ISBN978-3-0365-7926-9 (PDF)

This is a Reprint of the Special Issue Cancer Prevention with Molecular Target Therapies that was published in

Biology & Life Sciences
Chemistry & Materials Science
Medicine & Pharmacology
Summary

Personalized medicine plays an important role in cancer prevention. To date, it is clear that many cancers are molecularly distinct subtypes, and different therapeutic approaches would be required for each. Indeed, the identification of cancer susceptibility genes permits identifying patients “at risk” of developing neoplasia and supports modifying individual risk behaviors or the choice of preventive therapy. Additionally, the efficacy of various targeted therapies in different cancer subtypes suggests that treatment choices in the near future will be more and more centered on molecular signatures. Data from preclinical, clinical, and observational studies have revealed the ability to prevent cancer development for compounds with different indications than cancer. The concept of drug repurposing permits combinations that can target several critical pathways of a specific disease, decreasing the risk of resistance observed when using single-agent targeted therapy.This open-access Special Issue brings together original research and review articles on molecular oncology with attention to the early detection and prevention of cancer. It highlights new findings, methods, and technical advances in molecular cancer research. The main feature of this Special Issue is to provide an open-source sharing of significant works in the field of molecular oncology that can increase our understanding of cancer development, which may lead to the discovery of new molecular diagnostic technologies and targeted therapeutics.

Format
  • Hardback
License and Copyright
© 2022 by the authors; CC BY-NC-ND license
Keywords
melanoma; β3-tubulin; microtubules; microvesicles; endometrial cancer; steroid receptors; aromatase inhibitors; progression free survival; overall survival; ALK; EGFR; non-small-cell lung cancer (NSCLC); immune checkpoint inhibitor (ICI); adenocarcinoma; GANT61; non-canonical Hedgehog-GLI signaling; hepatocellular carcinoma; tyrosine kinase inhibitor; multidrug resistance; cancer; ABC transporter; SLC transporter; lysosomal sequestration; cancer cell migration; prognosis; biomarker; extracellular vesicles; lipid metabolism; human thymidylate synthase peptidic-inhibitors; pH-sensitive PEGylated liposomes; ovarian cancer; drug-resistance; raltitrexed; 5-fluorouracil; bladder cancer; muscle invasive; non-muscle invasive; molecular subtypes; evolution; targeted therapy; classification; gut microbiota; NAFLD; HCC; dysbiosis; metabolites; NSCLC; targeted therapy; early stage; EGFR; ALK; osimertinib; DMTF1; ARF; INK4a; p53; Cyclin D1; YY1; STAT3; cancer; tumor promoter; tumor suppressor