Small-cell lung cancer is characterized by a high incidence of deletions on chromosomes 3p, 4q, 5q, 10q, 13q and 17p - Wikidata - awgldk - TriplyDB

Small-cell lung cancer is characterized by a high incidence of deletions on chromosomes 3p, 4q, 5q, 10q, 13q and 17p

Small-cell lung cancer is characterized by a high incidence of deletions on chromosomes 3p, 4q, 5q, 10q, 13q and 17p

http://www.wikidata.org/entity/Q36419914

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DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumours Identification of a human homologue of the Schizosaccharomyces pombe rad17+ checkpoint gene Mapping of the gene for the human telomerase reverse transcriptase, hTERT, to chromosome 5p15.33 by fluorescence in situ hybridization Molecular biology of lung cancer: clinical implications Loss of HOP tumour suppressor expression in head and neck squamous cell carcinoma Chromosomal alterations in the clonal evolution to the metastatic stage of squamous cell carcinomas of the lung Lack of DMBT1 expression in oesophageal, gastric and colon cancers Small cell lung cancer (SCLC): no treatment advances in recent years Bronchopulmonary neuroendocrine tumors Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers Novel DNA copy number losses in chromosome 12q12--q13 in adenoid cystic carcinoma Gene expression profiling of advanced lung cancer.Chromosomal alterations in early stages of malignant mesotheliomas.Comparative genomic hybridization and chromosomal instability in solid tumours.Comparative genomic hybridization as a tool in tumour cytogenetics.LOH analysis of genes around D4S2964 identifies ARD1B as a prognostic predictor of hepatocellular carcinoma Array comparative genomic hybridization-based characterization of genetic alterations in pulmonary neuroendocrine tumors.Specific aneusomies in Chinese hamster cells at different stages of neoplastic transformation, initiated by nitrosomethylurea.Chromosome instability in human lung cancers: possible underlying mechanisms and potential consequences in the pathogenesis.Genetic imbalances with impact on survival in head and neck cancer patients.A novel target gene, SKP2, within the 5p13 amplicon that is frequently detected in small cell lung cancers.Typical and atypical carcinoid tumors of the lung are characterized by 11q deletions as detected by comparative genomic hybridization.DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies.DNA copy number changes in thyroid carcinoma Commentary: DNA base excision repair defects in human pathologies.Differential disruption of cell cycle pathways in small cell and non-small cell lung cancer.Mxi1 is a potential cellular target of carcinogens and frequently mutated in experimental rat tumors and tumor cell lines.Frequent genetic and biochemical alterations of the PI 3-K/AKT/PTEN pathway in head and neck squamous cell carcinoma.Functional evidence for a squamous cell carcinoma mortality gene(s) on human chromosome 4.Unravelling the biology of SCLC: implications for therapy.Combined MET inhibition and topoisomerase I inhibition block cell growth of small cell lung cancer.Overexpression of SERTAD3, a putative oncogene located within the 19q13 amplicon, induces E2F activity and promotes tumor growth.Centromeric chromosomal translocations show tissue-specific differences between squamous cell carcinomas and adenocarcinomas.Establishment and characterization of a human gastric carcinoma cell line TMC-1.Gene-expression profiling reveals distinct expression patterns for Classic versus Variant Merkel cell phenotypes and new classifier genes to distinguish Merkel cell from small-cell lung carcinoma.Chromosomal alterations in small cell lung cancer revealed by multicolour fluorescence in situ hybridization.CDKN2A is not the principal target of deletions on the short arm of chromosome 9 in neuroendocrine (Merkel cell) carcinoma of the skin.Analysis of chromosomal alterations in non-small cell lung cancer by multiplex-FISH, comparative genomic hybridization, and multicolor bar coding.Chromosomal changes during development and progression of prostate adenocarcinomas.Allelic loss on chromosome 10q in human lung cancer: association with tumour progression and metastatic phenotype.

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Small-cell lung cancer is characterized by a high incidence of deletions on chromosomes 3p, 4q, 5q, 10q, 13q and 17p

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British Journal of Cancer

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Dietel M

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P2860

The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers

An amino-terminal domain of Mxi1 mediates anti-Myc oncogenic activity and interacts with a homolog of the yeast transcriptional repressor SIN3

The MEL gene: a new member of the RAB/YPT class of RAS-related genes

Mutation of the MXI1 gene in prostate cancer

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

Loss of heterozygosity on chromosomes 3, 13, and 17 in small-cell carcinoma and on chromosome 3 in adenocarcinoma of the lung.

Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy.

Medical Research Council comparative trial of surgery and radiotherapy for primary treatment of small-celled or oat-celled carcinoma of bronchus. Ten-year follow-up.

Differential inactivation of CDKN2 and Rb protein in non-small-cell and small-cell lung cancer cell lines.

Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma.

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10.1038/BJC.1997.13

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