Promoter methylation of the hMLH1 gene and protein expression of human mutL homolog 1 and human mutS homolog 2 in resected esophageal squamous cell carcinoma [PDF]
Aberrant expression of mismatch repair genes, such as human mutL homolog 1 (hMLH1) and human mutS homolog 2 (hMSH2), are common in some human cancers, and promoter methylation is believed to inactivate expression of hMLH1. We investigated whether promoter methylation is involved in loss of hMLH1 protein and whether aberrant expression of hMLH1 and ...
Ho-Jui Tung +2 more
exaly +5 more sources
The GHKL ATPase Family as a Paradigm for MutL Homolog Function in DNA Mismatch Repair [PDF]
ATP hydrolysis drives essential processes across biology, from nucleic acid translocation and conformational switching to signal transduction. The GHKL ATPase family—DNA Gyrase B, Heat Shock Protein 90 (Hsp90), Histidine Kinases, and MutL homologs ...
Carol Manhart
exaly +3 more sources
Human Epidermal Growth Factor Receptor 2-Positive, Claudin-18 Isoform 2-Positive, Mismatch Repair-Deficient Gastric Cancer Revealed by Immunohistochemical Analysis of Surgical Specimens: A Case Report. [PDF]
ABSTRACT Background Human epidermal growth factor receptor 2 (HER2), mismatch repair (MMR) proteins, claudin‐18 isoform 2 (CLDN18.2), and the programmed cell death ligand‐1 combined positive score (PD‐L1 CPS) are predictive biomarkers for the efficacy of combination chemotherapy in patients with locally advanced unresectable or metastatic gastric or ...
Takagi D +10 more
europepmc +2 more sources
Background: The development of colorectal carcinoma is a complicated multistep process that involves the accumulation of mutations in tumor suppressor genes and oncogenes.
Eshita Garg +5 more
doaj +3 more sources
Mechanisms That Govern Recombinase Fidelity Control During Eukaryotic Homologous Recombination. [PDF]
The rate of recombinase filament formation controls the fidelity of the homologous recombination reaction by either restricting the length of strand pairing for high‐fidelity repair or increasing the length of strand pairing for more complex outcomes.
Korkmaz I, Crickard JB.
europepmc +2 more sources
Prognostic relevance of secondary actionable fusions in MLH1-deficient dMMR/MSI-H gastrointestinal tumors treated with pembrolizumab [PDF]
Background: Immune checkpoint inhibitors (ICIs) are standard treatment for mismatch repair-deficient (dMMR) or microsatellite instability-high (MSI-H) gastrointestinal tumors but resistance remains relevant.
N. Martínez Lago +10 more
doaj +2 more sources
The economic value of mismatch repair–guided immunotherapy in endometrial cancer: companion testing and patient selection [PDF]
Mismatch repair (MMR) status has moved from hereditary-cancer screening to a central predictive biomarker for immunotherapy in endometrial cancer. The marked difference in treatment benefit between MMR-deficient/microsatellite instability-high (dMMR/MSI ...
Sihan Jing, Yuan He, Yuan He, Yang Liu
doaj +2 more sources
Exome Sequencing Identifies Variants in MLH1 and ERBB2 as Potential Cancer-Predisposing Factors in Familial Early-Onset Colorectal Cancer. [PDF]
ABSTRACT Colorectal cancer (CRC) has raised considerable health concerns worldwide, with increasing incidence rates, specifically among younger populations. Despite remarkable progress in diagnosing and treating various diseases, the genetic basis of CRC remains only partially understood.
Bagheri B +7 more
europepmc +2 more sources
Most tumors, including osteosarcomas, have deficiencies in DNA damage repair. However, the regulatory mechanisms underlying dysregulation of DNA damage repair genes are still being investigated.
Xun Chen +7 more
doaj +1 more source
The methylation status of the O6-methylguanine methyltransferase (MGMT) gene promoter has been widely accepted as a prognostic biomarker for treatment with the alkylator, temozolomide (TMZ). In the absence of promoter methylation, the MGMT enzyme removes
Sachita Ganesa +3 more
doaj +1 more source

