Performance of capecitabine in novel combination therapies in colorectal cancer.
Antineoplastic Combined Chemotherapy Protocols
/ administration & dosage
Capecitabine
/ administration & dosage
Chemokines
/ biosynthesis
Colorectal Neoplasms
/ drug therapy
DNA Methylation
/ physiology
ErbB Receptors
/ antagonists & inhibitors
Humans
Proto-Oncogene Proteins B-raf
/ genetics
Proto-Oncogene Proteins p21(ras)
/ genetics
Proton Pump Inhibitors
/ administration & dosage
Receptor, ErbB-2
/ antagonists & inhibitors
Signal Transduction
Colorectal cancer
capecitabine
combination therapy
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
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