Pregled bibliografske jedinice broj: 1084912
Sphingosine 1-Phosphate Signaling and Metabolism in Chemoprevention and Chemoresistance in Colon Cancer
Sphingosine 1-Phosphate Signaling and Metabolism in Chemoprevention and Chemoresistance in Colon Cancer // Molecules, 25 (2020), 10; 2436-2457 doi:10.3390/molecules25102436 (međunarodna recenzija, članak, ostalo)
CROSBI ID: 1084912 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Sphingosine 1-Phosphate Signaling and
Metabolism in Chemoprevention and
Chemoresistance in Colon Cancer
Autori
Grbčić, Petra ; Sedić, Mirela
Izvornik
Molecules (1420-3049) 25
(2020), 10;
2436-2457
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, ostalo
Ključne riječi
chemoresistance ; colon cancer ; sphingolipid metabolism ; sphingosine 1-phosphate ; sphingosine kinases
Sažetak
Colorectal carcinoma (CRC) is the leading cause of cancer-related deaths worldwide. Despite advances in prevention and treatment modalities for CRC, rapidly developing resistance to chemotherapy limits its effectiveness. For that reason, it is important to better understand the mechanisms that undergird the process of chemoresistance to enable design of novel anticancer agents specifically targeting malignant properties of cancer cells. Over recent decades, bioactive sphingolipid species have come under the spotlight for their recognized role in cancer development and progression, and the evidence has surfaced to support their role as regulators of anti-cancer drug resistance. Colon cancer is characterized by a shift in sphingolipid balance that favors the production and accumulation of oncogenic species such as sphingosine 1-phosphate (S1P). S1P is known to govern the processes that facilitate cancer cell growth and progression including proliferation, survival, migration, invasion and inflammation. In this review paper, we will give a comprehensive overview of current literature findings on the molecular mechanisms by which S1P turnover, transport and signaling via receptor-dependent and independent pathways shape colon cancer cell behavior and influence treatment outcome in colon cancer. Combining available modulators of S1P metabolism and signaling with standard chemotherapy drugs could provide a rational approach to achieve enhanced therapeutic response, diminish chemoresistance development and improve the survival outcome in CRC patients.
Izvorni jezik
Engleski
POVEZANOST RADA
Projekti:
HRZZ-IP-2018-01-3900 - Rasvijetljavanje mehanizama rezistencije na terapiju raka debelog crijeva sa mutacijom BRAF pomoću integriranog -omics pristupa (BRAFCON) (Sedić, Mirela, HRZZ - 2018-01) ( CroRIS)
Ustanove:
Sveučilište u Rijeci - Odjel za biotehnologiju
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE