Performance of capecitabine in novel combination therapies in colorectal cancer.


Journal

Journal of chemotherapy (Florence, Italy)
ISSN: 1973-9478
Titre abrégé: J Chemother
Pays: England
ID NLM: 8907348

Informations de publication

Date de publication:
Oct 2021
Historique:
pubmed: 22 5 2021
medline: 18 1 2022
entrez: 21 5 2021
Statut: ppublish

Résumé

Colorectal cancer is one of the most common cancers throughout the world, and no definitive cure has ever been found. Perhaps a new insight into the effectiveness of chemotherapy drugs could help better treat patients. Targeted therapies have significantly improved the median overall survival of colorectal cancer patients. One of the standard chemotherapy regimens used for colorectal cancer is capecitabine, which is important in monotherapy and combination therapies. Capecitabine, with other chemotherapeutic agents (irinotecan, oxaliplatin, perifosine, 17-allylamino-17-demethoxygeldanamycin, aspirin, celecoxib, statins, quinacrine, inositol hexaphosphate and inositol, cystine/theanine, curcumin, and isorhamnetin), and biological ones (antibodies) plays an important role in the inhibition of some signaling pathways, increasing survival, reducing tumor growth and side effects of capecitabine. However, some drugs, such as proton pump inhibitors, are negatively related to capecitabine; therefore, the purpose of this work is to review and discuss the performance of capecitabine combination therapies in colorectal cancer.

Identifiants

pubmed: 34019782
doi: 10.1080/1120009X.2021.1920247
doi:

Substances chimiques

Chemokines 0
KRAS protein, human 0
Proton Pump Inhibitors 0
Capecitabine 6804DJ8Z9U
ERBB2 protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1
BRAF protein, human EC 2.7.11.1
Proto-Oncogene Proteins B-raf EC 2.7.11.1
Proto-Oncogene Proteins p21(ras) EC 3.6.5.2

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

375-389

Auteurs

Fahima Danesh Pouya (FD)

Department of Biochemistry, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.

Yousef Rasmi (Y)

Department of Biochemistry, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Cellular and Molecular Research Center, Urmia University of Medical Sciences, Urmia, Iran.

Irem Yalim Camci (IY)

Department of Molecular Biology and Genetics, Faculty of Science, Gebze Technical University, Kocaeli, Turkey.

Yusuf Tutar (Y)

Division of Biochemistry, Department of Basic Pharmaceutical Sciences, Hamidiye Faculty of Pharmacy, University of Health Sciences, Turkey Istanbul.

Mohadeseh Nemati (M)

Department of Biochemistry, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.

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Classifications MeSH