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Leukemia Research
Volume 27, Issue 7
, Pages 627-633
, July 2003
Coincidental LOH regions in mouse and humans: evidence for novel tumor suppressor loci at 9q22–q34 in non-Hodgkin’s lymphomas
References
-
.
Allelotyping of butadiene-induced lung and mammary adenocercinomas of B6C3F1 mice: frequent losses of heterozygosity in regions homologous to human tumor-suppressor genes.
Proc. Natl. Acad. Sci. U.S.A. 1994;91:3759–3763
-
.
Loss of heterozygosity on chromosomes 1, 11, 12 and 14 in hybrid mouse lung adenocarcinomas.
Mol. Carcinogenesis. 1996;16:83–90
- . Evidence of a possible epigenetic inactivation mechanism operating on a region of mouse chromosome 19 in γ-radiation-induced thymic lymphomas. Oncogene. 1996;12:669–676
- . A new candidate site for a tumor suppressor gene involved in mouse thymic lymphomagenesis is located on the distal part of chromosome 4. Oncogene. 1998;17:925–929
- . Evidence of a possible epigenetic inactivation mechanism operating on a region of mouse chromosome 19 in gamma-radiation-induced thymic lymphomas. Oncogene. 2001;20:2186–2189
- . Allelotype analysis of 2′,3′-dideoxycytidine- and 1,3-butadiene-induced lymphomas in B6C3F1 mice. Cancer Res. 1996;56:3338–3343
- . Loss of heterozygosity at the proximal-mid part of mouse chromosome 4 defines two novel tumor suppressor gene loci in T-cell lymphomas. Oncogene. 1999;18:4166–4169
- . The p16INK4a/CDKN2A tumor suppressor and its relatives. Biochim. Biophys. Acta. 1998;1378:F115–F177
- . Frequent loss of heterozygosity on chromosomes 4, 12 and 19 in radiation-induced lymphomas in mice. Cancer Lett. 1999;135:223–228
- . Analysis of highly frequent allelic loss region on distal chromosome 12 in murine radiation-induced lymphomas. Cancer Lett. 2000;148:95–103
- . Allelotype analysis of chemically induced squamous cell carcinomas in F1 hybrids of two inbred mouse strains with different susceptibility to tumor progression. Carcinogenesis. 2000;21:1297–1301
- PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science. 1997;275:1943–1947
- . IgH, TCR-gamma, and TCR-beta gene rearrangement in 80 B- and T-cell non-Hodgkin’s lymphomas: study of the association between proliferation and the so-called “aberrant” patterns. Diagn. Mol. Pathol. 2000;10:69–77
-
Frequent allelic losses of 9p21 markers and low incidence of mutations at p16CDKN2 gene in non-Hodgkin lymphomas of B-cell lineage.
Cancer Genet. Cytogenet. 1997;981:63–68
- Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumors. Cancer Res. 1997;57:4710–4713
- . PTEN/MMAC1 mutations in endometrial cancers. Cancer Res. 1997;57:4736–4738
- Hypermethylation of a 5′ CpG island of p16 is a frequent event in non-Hodgkin’s lymphoma. Leukemia. 1997;11:425–428
- . Diffuse large cell lymphomas exhibit frequent deletions in 9p21–22 and 9q31–34 regions. Genes Chromosomes Cancer. 1995;12:32–36
- Evidence for two tumor suppressor loci associated with proximal chromosome 9p to q and distal chromosome 9q in bladder cancer and the initial screening for Gas1 and PTC mutations. Cancer Res. 1996;56:5039–5043
- . Structure and methylation-based silencing of a gene DBCCR1 within a candidate bladder cancer tumor suppressor region at 9q32–q33. Genomics. 1998;48:277–288
- . PTCH gene mutations in invasive transitional cell carcinoma of the bladder. Oncogene. 1998;17:1167–1172
-
.
A deletion in the gene for transforming growth factor β type I receptor abolishes growth regulation by transforming growth factor β in a cutaneous T-cell lymphoma.
Blood. 1999;8:2854–2861
- CDKN2A is not the principal target of deletions on the short arm of chromosome 9 in neuroendocrine Merkel cell carcinoma of the skin. Int. J. Cancer. 2001;93:361–367
- . Evidence for three tumor suppressor loci on chromosome 9p involved in melanoma development. Cancer Res. 2001;61:1154–1161
- . Deletion mapping of chromosomal region 1p32-pter in primary breast cancer. Genes Chromosomes Cancer. 1999;24:255–263
- Frequent loss of heterozygosity at 1p36 in ovarian adenocarcinomas but gene encoding p73 is unlikely to be the target. Oncogene. 1999;18:4640–4642
- Chromosome bands 1p35–36 contain two distinct neuroblastoma tumor suppressor loci, one of which is imprinted. Genes Chromosomes Cancer. 2001;30:168–174
- Allelic losses and genetic instabilities of PTEN and p73 in non-Hodgkin lymphomas. Leukemia. 2000;14:1325–1327
- Frequent inactivation of the p73 gene by abnormal methylation or LOH in non-Hodgkin’s lymphomas. Int. J. Cancer. 2002;102:15–19
- Transcriptional silencing of the p73 gene in acute lymphoblastic leukemia and Burkitt’s lymphoma is associated with 5′ CpG island methylation. Cancer Res. 1999;59:3352–3356
- Altered PTEN expression as a diagnostic marker for the earliest endometrial precancers. J. Natl. Cancer Inst. 2000;92:924–930
- . Alterations of the MMAC1/PTEN gene in lymphoid malignancies. Blood. 1998;91:4388–4390
- . PTEN gene alterations in lymphoid neoplasms. Blood. 1998;92:3410–3415
- . Analysis of PTEN mutations and deletions in B-cell non-Hodgkin’s lymphomas. Genes Chromosomes Cancer. 1999;24:322–327
- Deletions in the long arm of chromosome 10 in lymphomas with t14;18: a pathogenetic role of the tumor suppressor genes PTEN/MMAC1 and MXI1?. Blood. 1998;92:4487–4489
- . Loss of heterozygosity on 10q and microsatellite instability in advanced stages of primary cutaneous T-cell lymphoma and possible association with homozygous deletion of PTEN. Blood. 2000;95:2937–2942
- Genetic instability of microsatellites in hematological neoplasms. Leukemia. 1995;9:960–964
-
.
Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation.
Nature Genet. 1994;6:273–281
-
Cañamero M. Linfomas tı́micos murinos inducidos con radiación gamma: caracterización morfológica, IHQ, ultraestructural y genética. Madrid: Universidad Autónoma de Madrid, 2001.
- . Allelic loss on chromosome 4 Lyr2/TLSR5 is associated with myeloid, B-lympho-myeloid, and lymphoid B and T mouse radiation-induced leukemias. Blood. 2001;98:1549–1554
- Analysis of loss of heterozygosity in lymphoma and leukemia arising in F1 hybrid mice locates a common region of chromosome 4 loss. Genes Chromosomes Cancer. 2001;31:373–381
PII: S0145-2126(02)00278-3
doi: 10.1016/S0145-2126(02)00278-3
© 2003 Elsevier Science Ltd. All rights reserved.
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Leukemia Research
Volume 27, Issue 7
, Pages 627-633
, July 2003
