Literature DB >> 26845137

Fibroblast Growth Factor Receptor (FGFR): A New Target for Non-small Cell Lung Cancer Therapy.

Federica Biello1, Giovanni Burrafato, Erika Rijavec, Carlo Genova, Giulia Barletta, Anna Truini, Simona Coco, Maria Giovanna Dal Bello, Angela Alama, Francesco Boccardo, Francesco Grossi.   

Abstract

Lung cancer is still the leading cause of cancer related death worldwide. Fibroblast growth factor receptor (FGFR) is a tirosine-kinase receptor that is seen to be amplified or mutated in non-small cell lung cancer (NSCLC) and it plays a crucial role in tumour development and maintenance. The authors analyzed the state of the art of FGFR by reviewing the current literature. Fibroblast growth factor (FGF)-FGFR pathway and their aberrations are described, with the evaluation of their possible prognostic role in NSCLC and in particular in squamous cell carcinomas, in which FGFR is more often amplified. New therapeutic agents targeting FGFR signaling have been developed and are now in clinical evaluation. Dysregulation of FGF signaling in tumour cells is related to FGFR gene amplification or mutation, although it is still uncertain which of these aberrations represents a real predictor of response to specific inhibitors. However, recent evidence has questioned whether FGFR is a real target in squamous cell histology. The effectiveness of FGFR inhibitors is also still unclear since there are no clinical data on selected patients. Moreover, the management of specific side effects related to inhibition of the physiological role of FGF should be more thorough.

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Year:  2016        PMID: 26845137     DOI: 10.2174/1871520616666160204112347

Source DB:  PubMed          Journal:  Anticancer Agents Med Chem        ISSN: 1871-5206            Impact factor:   2.505


  5 in total

1.  Fibroblast growth factor receptor 1 and 3 expression is associated with regulatory PI3K/AKT kinase activity, as well as invasion and prognosis, in human laryngeal cancer.

Authors:  Katarzyna Starska; Ewa Forma; Iwona Lewy-Trenda; Olga Stasikowska-Kanicka; Michał Skóra; Magdalena Bryś
Journal:  Cell Oncol (Dordr)       Date:  2018-01-03       Impact factor: 6.730

2.  Etiologic Role of Kinases in the Progression of Human Cancers and Its Targeting Strategies.

Authors:  Sanjoy Das; Bireswar Bhattacharya; Biplajit Das; Bibek Sinha; Taison Jamatia; Kishan Paul
Journal:  Indian J Surg Oncol       Date:  2019-08-19

3.  The inhibition of FGF receptor 1 activity mediates sorafenib antiproliferative effects in human malignant pleural mesothelioma tumor-initiating cells.

Authors:  Alessandra Pattarozzi; Elisa Carra; Roberto E Favoni; Roberto Würth; Daniela Marubbi; Rosa Angela Filiberti; Luciano Mutti; Tullio Florio; Federica Barbieri; Antonio Daga
Journal:  Stem Cell Res Ther       Date:  2017-05-25       Impact factor: 6.832

4.  C1632 suppresses the migration and proliferation of non-small-cell lung cancer cells involving LIN28 and FGFR1 pathway.

Authors:  Jing-Yi Chen; Yu-Jing Chen; Lu Liu; Xiang-Xiang Jin; Zhe Shen; Wen-Bin Chen; Teng Yang; Si-Bei Xu; Guang-Bao Wang; Yi-Nuo Cheng; De-Zhi Cheng; Zhi-Guo Liu; Xiao-Hui Zheng
Journal:  J Cell Mol Med       Date:  2021-12-16       Impact factor: 5.310

5.  Bruceine H Mediates EGFR-TKI Drug Persistence in NSCLC by Notch3-Dependent β-Catenin Activating FOXO3a Signaling.

Authors:  Jiahui Wu; Xiao He; Ziwei Xiong; Lingyu Shi; Daofeng Chen; Yulin Feng; Quan Wen
Journal:  Front Oncol       Date:  2022-04-08       Impact factor: 5.738

  5 in total

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