2011
DOI: 10.1016/s1348-8643(11)00027-9
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Loss of heterozygosity in oral cancer

Abstract: a b s t r a c tThe development and progression of oral squamous cell carcinoma (OSCC) is a multistep process, which involves many genetic factors. Among them, loss of heterozygosity (LOH) studies have been used to identify regions on chromosomes that may contain putative tumor suppressor genes (TSGs). Here, we searched PubMed for relevant publications including our previous studies and compared results of LOH in OSCCs from the articles. LOHs in OSCCs were observed at various loci on almost all chromosomes, exc… Show more

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Cited by 17 publications
(14 citation statements)
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References 77 publications
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“…These histologic response rates compare favorably with other chemoprevention trials . LOH is thought to facilitate tumorigenesis via the monoallelic inactivation of tumor suppressor genes . The results of the LOH evaluation before and after gel treatment showed that a local drug delivery strategy significantly reduces LOH .…”
Section: Advances In Drug Delivery Systemssupporting
confidence: 57%
“…These histologic response rates compare favorably with other chemoprevention trials . LOH is thought to facilitate tumorigenesis via the monoallelic inactivation of tumor suppressor genes . The results of the LOH evaluation before and after gel treatment showed that a local drug delivery strategy significantly reduces LOH .…”
Section: Advances In Drug Delivery Systemssupporting
confidence: 57%
“…Loss of heterozygosity (LOH) occurs in a somatic cell upon loss of genomic material specifically within the only remaining copy of a functional allele. LOH patterns have been found in OSCC samples at various loci across all chromosomes, except X and Y . Most notably, LOH has been observed on chromosomal arms 3p, 9p, 13q, and 17p at the earliest stages of oral carcinogenesis .…”
Section: Molecular Markersmentioning
confidence: 99%
“…Analysis of loss of heterozygosity (LOH) is one of the common methods used to molecular study of premalignant lesions and was previously used for detection of molecular abnormalities in HNSCC . As a result of this analysis, almost 6000 variants in all cellular groups were observed.…”
Section: Resultsmentioning
confidence: 99%