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Cysteinyl Leukotriene Pathway and Cancer.

Abstract
Cancer remains a leading cause of death worldwide, despite many advances being made in recent decades. Changes in the tumor microenvironment, including dysregulated immunity, may contribute to carcinogenesis and cancer progression. The cysteinyl leukotriene (CysLT) pathway is involved in several signal pathways, having various functions in different tissues. We summarized major findings of studies about the roles of the CysLT pathway in cancer. Many in vitro studies suggested the roles of CysLTs in cell survival/proliferation via CysLT1 receptor (CysLT1R). CysLT1R antagonism decreased cell vitality and induced cell death in several types of cancer cells, such as colorectal, urological, breast, lung and neurological malignancies. CysLTs were also associated with multidrug resistance of cancer, and CysLT1R antagonism might reverse chemoresistance. Some animal studies demonstrated the beneficial effects of CysLT1R antagonist in inhibiting tumorigenesis and progression of some cancer types, particularly colorectal cancer and lung cancer. The expression of CysLT1R was shown in various cancer tissues, particularly colorectal cancer and urological malignancies, and higher expression was associated with a poorer prognosis. The chemo-preventive effects of CysLT1R antagonists were demonstrated in two large retrospective cohort studies. In summary, the roles of the CysLT pathway in cancer have been delineated, whereas further studies are still warranted.
AuthorsMing-Ju Tsai, Wei-An Chang, Cheng-Hao Chuang, Kuan-Li Wu, Chih-Hung Cheng, Chau-Chyun Sheu, Ya-Ling Hsu, Jen-Yu Hung
JournalInternational journal of molecular sciences (Int J Mol Sci) Vol. 23 Issue 1 (Dec 23 2021) ISSN: 1422-0067 [Electronic] Switzerland
PMID35008546 (Publication Type: Journal Article, Review)
Chemical References
  • Leukotrienes
  • cysteinyl-leukotriene
  • Cysteine
Topics
  • Animals
  • Apoptosis (physiology)
  • Cell Proliferation (physiology)
  • Cysteine (metabolism)
  • Humans
  • Leukotrienes (metabolism)
  • Neoplasms (metabolism)
  • Retrospective Studies
  • Signal Transduction (physiology)

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