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Signaling Pathways Dysregulation in Cancer: Advances and New Therapeutics Hopes

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Oncology".

Deadline for manuscript submissions: 31 August 2024 | Viewed by 2325

Special Issue Editor


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Guest Editor
Department of Biochemistry, Faculty of Dentistry, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania
Interests: PI3K/AKT/mTOR; oxidative stress; breast cancer; burns; colorectal cancer; PLGA nanoparticles; platelet rich plasma
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Special Issue Information

Dear Colleagues,

Malignant neoplasms, characterized by successive genetic and epigenetic alterations of healthy cells, are one of the leading causes of death within the adult population. Usually, most cancers emerge at the epithelial cells, leading to organ-specific carcinomas affecting skin, liver, lung, breast, or pancreas. Since oncogenic mutations induce gene overexpression and subsequently cause protein dysregulation, the PI3K/AKT/mTOR, TGF-β family, Ras/Raf/MEK/ERK, and the Wnt/β-catenin signaling pathway dysregulations are correlated with the proliferation, angiogenesis, invasion, and metastasis of cancer cells. Therefore, inhibitors targeting these pathways are considered as novel therapeutic candidates for the development of potential anticancer agents.

We cordially invite submissions of original research and comprehensive review articles for inclusion in this Special Issue.

This Special Issue is overseen by Dr. Daniela Miricescu with the assistance of Dr. Constantin Stefani ( Department of Family Medicine and Clinical Base, Dr. Carol Davila Central Military Emergency University Hospital).

Dr. Daniela Miricescu
Guest Editor

Manuscript Submission Information

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Keywords

  • cancer
  • epithelial cells
  • oncogenic mutations
  • PI3K/AKT/mTOR
  • TGF-β
  • Ras/Raf/MEK/ERK
  • Wnt/β-catenin
  • angiogenesis
  • invasion
  • metastasis
  • inhibitors

Published Papers (1 paper)

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Review

26 pages, 1785 KiB  
Review
Targeting PI3K/AKT/mTOR and MAPK Signaling Pathways in Gastric Cancer
by Diana-Theodora Morgos, Constantin Stefani, Daniela Miricescu, Maria Greabu, Silviu Stanciu, Silvia Nica, Iulia-Ioana Stanescu-Spinu, Daniela Gabriela Balan, Andra-Elena Balcangiu-Stroescu, Elena-Claudia Coculescu, Dragos-Eugen Georgescu and Remus Iulian Nica
Int. J. Mol. Sci. 2024, 25(3), 1848; https://doi.org/10.3390/ijms25031848 - 03 Feb 2024
Viewed by 2018
Abstract
Gastric cancer (GC) is the fourth leading cause of death worldwide, with more than 1 million cases diagnosed every year. Helicobacter pylori represents the main risk factor, being responsible for 78% of the cases. Increased amounts of salt, pickled food, red meat, alcohol, [...] Read more.
Gastric cancer (GC) is the fourth leading cause of death worldwide, with more than 1 million cases diagnosed every year. Helicobacter pylori represents the main risk factor, being responsible for 78% of the cases. Increased amounts of salt, pickled food, red meat, alcohol, smoked food, and refined sugars negatively affect the stomach wall, contributing to GC development. Several gene mutations, including PIK3CA, TP53, ARID1A, CDH1, Ras, Raf, and ERBB3 are encountered in GC pathogenesis, leading to phosphatidylinositol 3-kinase (PI3K) protein kinase B (AKT)/mammalian target of rapamycin (mTOR)—PI3K/AKT/mTOR—and mitogen-activated protein kinase (MAPK) signaling pathway activation and promoting tumoral activity. Helicobacter pylori, growth factors, cytokines, hormones, and oxidative stress also activate both pathways, enhancing GC development. In clinical trials, promising results have come from monoclonal antibodies such as trastuzumab and ramucirumab. Dual inhibitors targeting the PI3K/AKT/mTOR and MAPK signaling pathways were used in vitro studies, also with promising results. The main aim of this review is to present GC incidence and risk factors and the dysregulations of the two protein kinase complexes together with their specific inhibitors. Full article
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