Results 31 to 40 of about 5,903 (227)
Pharmacogenomic-guided dosing of fluoropyrimidines beyond DPYD: time for a polygenic algorithm?
Fluoropyrimidines are chemotherapeutic agents widely used for the treatment of various solid tumors. Commonly prescribed FPs include 5-fluorouracil (5-FU) and its oral prodrugs capecitabine (CAP) and tegafur.
Anthi Maslarinou +6 more
doaj +1 more source
Management of cytotoxic chemotherapy-induced hand-foot syndrome
Improvements in systemic cancer treatments have resulted in more patients surviving for prolonged periods of time on treatment. This has made treatment-related toxicity and quality of life concerns increasingly relevant.
Johannes J.M. Kwakman +3 more
doaj +1 more source
(A) Evaluation of the supernatants’ impact on the colony growth of strains on solid medium. (B) Microtiter-based hyphal growth quantification and (C) representative microscopic images illustrating growth of strains in liquid AMM supplemented with ...
Luis Enrique Sastré-Velásquez (14305295) +7 more
core +1 more source
Background Fluoropyrimidines (FP) are among the most common class of prescribed anti‐neoplastic drugs. This class has severe to moderate toxicity in around 10%–40% of those who take 5‐fluorouracil (5‐FU) or capecitabine for the treatment of cancer.
Hatouf H. Sukkarieh +7 more
doaj +1 more source
There are clinical challenges related to adjuvant treatment in colorectal cancer (CRC) and novel molecular markers are needed for better risk stratification of patients.
Elena De Mattia +16 more
doaj +1 more source
Dutch Pharmacogenetics Working Group (DPWG) guideline for the gene–drug interaction of DPYD and fluoropyrimidines [PDF]
Despite advances in the field of pharmacogenetics (PGx), clinical acceptance has remained limited. The Dutch Pharmacogenetics Working Group (DPWG) aims to facilitate PGx implementation by developing evidence-based pharmacogenetics guidelines to optimize ...
Schaik, R.H.N. (Ron) van +14 more
core +6 more sources
Background: The fluoropyrimidine anticancer drug, especially 5- fluorouracil (5-FU) and its prodrug capecitabine are still being the backbone of chemotherapeutic regimens for colorectal cancer.
Chi C. Tong +4 more
doaj +1 more source
Thymidylate synthase (TS) catalyzes methylation of dUMP to dTMP and it is the target for the 5-Fluorouracil (5-FU) activity. Barbour et al.
A. Calascibetta +7 more
doaj +1 more source
Model illustrating the proposed mechanism by which chemotherapy‐induced downregulation of OGT disrupts SNAP29 O‐GlcNAcylation, promoting STX17‐SNAP29‐VAMP8 SNARE complex assembly and protective autophagy, leading to chemoresistance, which in turn establishes a feedforward loop to perpetuate drug tolerance.
Liang Tang +9 more
wiley +1 more source
DPYD pathogenic variants associated with fluoropyrimidines toxicity [PDF]
Background: Genetic variants in dihydropyrimidine dehydrogenase gene (DPYD) coding for the key enzyme (DPD) of fluoropyrimidines (FPs) catabolism. DPYD contributes to the development of severe FPs-related toxicity, and pathogenic DPYD variants detection ...
Burciaga-Flores, Carlos Horacio +9 more
core +1 more source

