SEMA6B IS A CANDIDATE TUMOR SUPPRESSOR GENE IN THE CRITICAL CHROMOSOME REGION 19P13.3
https://doi.org/10.1234/XXXX-XXXX-2013-2-32-36
Abstract
Numerous studies indicate an extremely high rate of loss of heterozygosity on the short arm of chromosome 19, in the chromosomal segment 19p13.3, for different types of neoplasia: coion, cervical, breast cancers, myeloid leukemia. High rates of 19p13.3 loss of heterozygosity suggest that it contains one or more tumor suppressor genes. Our study of molecular pathology of the SEMA6B gene located in a critical area in breast cancer samples reveals features characteristic of the tumor suppressor gene. The frequency of abnormal methylation of the 5' region of the gene and the rate of loss of heterozygosity in breast cancer samples equal correspondingly 38% and 50%. A germinal mutation in an evolutionarily conserved region of the SEMA6B gene was detected in one of the breast cancer patients.
About the Authors
E. B. KuznetsovaRussian Federation
E. A. Pudova
Russian Federation
A. S. Tanas
Russian Federation
D. V. Zaletaev
Russian Federation
V. V. Strelnikov
Russian Federation
References
1. Кузнецова Е.Б., Дрозд О.В., Бабенко О.В., Землякова В.В., Немцова М.В., Залетаев Д.В., Стрельников В.В. Идентификация генов, вовлеченных в канцерогенез, методом метилчувствительного ПЦР-фингерпринтинга // Медицинская генетика. — 2004. — Т. 3, №12. — С. 563—568.
2. Кузнецова Е.Б., Кекеева Т.В., Ларин С.С., Землякова В.В., Бабенко О.В., Немцова М.В., Залетаев Д.В., Стрельников В.В. Новые маркёры метилирования и экспрессии генов при раке молочной железы // Молекулярная биология. — 2007. — Т. 41, №4. — С. 624?633.
3. Basile J.R., Holmbeck K., Bugge T.H., Gutkind J.S. MT1-MMP Controls Tumor-induced Angiogenesis through the ReHislease of Semaphorin 4D // J. Biol. Chem. — 2007. — Vol. 282. — P. 6899—6905.
4. Christensen C., Ambartsumian N., Gilestro G. et al. Proteolytic Processing Converts the Repelling Signal Sema3E into an Inducer of Invasive Growth and Lung Metastasis // Cancer Res. — 2005. — Vol. 65. — P. 6167—6177.
5. Connolly D.C., Katabuchi H., Cliby W.A. Cho K.R. Somatic Mutations in the STK11/LKB1 Gene Are Uncommon in Rare Gynecological Tumor Types Associated with Peutz-Jegher’s Syndrome // Am. J. Pathol. — 2000. — Vol. 156. — P. 339.
6. Forster L.F., Defres S., Goudie D.R., Baty D.U., Carey F.A. An investigation of the Peutz-Jeghers gene (LKB1) in sporadic breast and colon cancers // J. Clin. Pathol. — 2000. — Vol. 53. — P. 791—793.
7. Futamura M., Kamino H., Miyamoto Y. et al. Possible Role of Semaphorin 3F, a Candidate Tumor Suppressor Gene at 3p21.3, in p53-Regulated Tumor Angiogenesis Suppression // Cancer Res. — 2007. — Vol. 67. — P. 1451—1460.
8. Futreal P.A., Coin L., Marshall M. et al. A census of human cancer genes // Nat. Rev. Cancer. — 2004. — Vol. 4(3). — P. 177—183.
9. Kuroki T., Trapasso F., Yendamuri S. et al. Allelic Loss on Chromosome 3p21.3 and Promoter Hypermethylation of Semaphorin 3B in Non-Small Cell Lung Cancer // Cancer Res. — 2003. — Vol. 63. — P. 3352—3355.
10. Lee J.Y., Dong S.M., Kim H.S. et al. Distinct Region of Chromosome 19p 13.3 Associated with the Sporadic Form of Adenoma Malignum of the Uterine Cervix // Cancer Res. — 1998. — Vol. 58. — P. 1140—1143.
11. Oesterreich S., Allredl D.C., Mohsin S.K. et al. High rates of loss of heterozygosity on chromosome 19p13 in human breast cancer // Br. J. Cancer. — 2001. — Vol. 84(4). — P. 493—498.
12. Puttagunta R., Gordon L.A., Meyer G.E. et al. Comparative Maps of Human 19p 13.3 and Mouse Chromosome 10 Allow Identification of Sequences at Evolutionary Breakpoints // Genome Res. — 2000. — Vol. 10. — P. 1369—1380.
13. Qu X., Wei H., Zhai Y. et al. Identification, Characterization, and Functional Study of the Two Novel Human Members of the Semaphorin Gene Family // J. Biol. Chem. — 2002. — Vol. 277. — P. 35574—35585.
14. Resta N., Simone C., Mareni C., Montera M., Gentile M., et at. STK11 Mutations in Peutz-Jeghers Syndrome and Sporadic Colon Cancer // Cancer Res. — 1998. — Vol. 58. — P. 4799—4801.
15. Sanlalius T., Shipley J., Brewer D., Stratton M.R., Cooper C.S. A census of amplified and overexpressed human cancer genes // Nat. Rev. Cancer. — 2010. — Vol. 10(1). — P. 59—64.
16. Stratton M.R. Exploring the Genomes of Cancer Cells: Progress and Promise // Science. — 2011. — Vol. 331. — P. 1553—1558.
17. Tanas A.S., Shkarupo V.V, Kuznetsova E.B., Zaletay-ev D.V., Strelnikov V.V. Novel tools for unbiased DNA differential methylation screening // Epigenomics. — 2010. — Vol. 2, №2. — P. 325—333.
18. Taniwaki B.M., Nishida K., Takashirna T., Nakagawa H. et al. Nonrandom Chromosomal Rearrangements of 14q32.3 and 19р13.3 and Preferential Deletion of lp in 21 Patients With Multiple Myeloma and Plasma Cell Leukemia // Blood. — 1994. — Vol 84, №7. — P. 2283—2290.
19. Wang Z.-J., Churchman M., Campbell I.G. et al. Allele loss and mutation screen at the Peutz-Jeghers (LKB1) locus (19p13.3) in sporadic ovarian tumours // Br. J. Cancer. — 1999. — Vol. 80(1/2). — P. 70—72.
20. Yang T.L., Su Y.R., Huang C.S., Yu J.C., Lo Y.L., Wu P.E., Shen C.Y. High-resolution 19p13.2-13.3 allelotyping of breast carcinomas demonstrates frequent loss of heterozygosity // Genes Chromosomes Cancer. — 2004. — Vol. 41(3). — P. 250—256.
Review
For citations:
Kuznetsova E.B., Pudova E.A., Tanas A.S., Zaletaev D.V., Strelnikov V.V. SEMA6B IS A CANDIDATE TUMOR SUPPRESSOR GENE IN THE CRITICAL CHROMOSOME REGION 19P13.3. Medical Genetics. 2013;12(2):32-36. (In Russ.) https://doi.org/10.1234/XXXX-XXXX-2013-2-32-36