Cell cycle in sporadic melanoma
Sporadic melanoma is a neoplasm whose etiology has not been fully investigated. Contemporary achievements in molecular biology have made it possible to localize the genes whose damage can contribute to the initiation of neoplastic transformation of melanocytes and lead to a progression of the diseas...
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Published in | International journal of dermatology Vol. 41; no. 9; pp. 550 - 556 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Science Ltd
01.09.2002
Blackwell Science Blackwell Publishing Ltd |
Subjects | |
Online Access | Get full text |
ISSN | 0011-9059 1365-4632 |
DOI | 10.1046/j.1365-4362.2002.01601.x |
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Abstract | Sporadic melanoma is a neoplasm whose etiology has not been fully investigated. Contemporary achievements in molecular biology have made it possible to localize the genes whose damage can contribute to the initiation of neoplastic transformation of melanocytes and lead to a progression of the disease. The majority of these genes are responsible for the correct progression of phase G1 of the cell cycle. Phase G1 of the cell cycle is subject to control by many protooncogenes and antioncogenes, which constitute the pRb or p53 pathway, damage to which can lead to the development of malignant melanoma. The present paper discusses disorders in the control of phase G1 of the cell cycle in sporadic melanoma. |
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AbstractList | Sporadic melanoma is a neoplasm whose etiology has not been fully investigated. Contemporary achievements in molecular biology have made it possible to localize the genes whose damage can contribute to the initiation of neoplastic transformation of melanocytes and lead to a progression of the disease. The majority of these genes are responsible for the correct progression of phase G1 of the cell cycle. Phase G1 of the cell cycle is subject to control by many protooncogenes and antioncogenes, which constitute the pRb or p53 pathway, damage to which can lead to the development of malignant melanoma. The present paper discusses disorders in the control of phase G1 of the cell cycle in sporadic melanoma. Sporadic melanoma is a neoplasm whose etiology has not been fully investigated. Contemporary achievements in molecular biology have made it possible to localize the genes whose damage can contribute to the initiation of neoplastic transformation of melanocytes and lead to a progression of the disease. The majority of these genes are responsible for the correct progression of phase G1 of the cell cycle. Phase G1 of the cell cycle is subject to control by many protooncogenes and antioncogenes, which constitute the pRb or p53 pathway, damage to which can lead to the development of malignant melanoma. The present paper discusses disorders in the control of phase G1 of the cell cycle in sporadic melanoma.Sporadic melanoma is a neoplasm whose etiology has not been fully investigated. Contemporary achievements in molecular biology have made it possible to localize the genes whose damage can contribute to the initiation of neoplastic transformation of melanocytes and lead to a progression of the disease. The majority of these genes are responsible for the correct progression of phase G1 of the cell cycle. Phase G1 of the cell cycle is subject to control by many protooncogenes and antioncogenes, which constitute the pRb or p53 pathway, damage to which can lead to the development of malignant melanoma. The present paper discusses disorders in the control of phase G1 of the cell cycle in sporadic melanoma. |
Author | Czajkowski, Rafał Krzyżyńska-Malinowska, Ewa Drewa, Tomasz Woźniak, Alina |
Author_xml | – sequence: 1 givenname: Rafał surname: Czajkowski fullname: Czajkowski, Rafał email: rafal.czajkowski@pf.pl organization: From the Departments of Dermatology and – sequence: 2 givenname: Tomasz surname: Drewa fullname: Drewa, Tomasz organization: Biology, Ludwik Rydygier Medical University, Bydgoszcz, Poland – sequence: 3 givenname: Alina surname: Woźniak fullname: Woźniak, Alina organization: Biology, Ludwik Rydygier Medical University, Bydgoszcz, Poland – sequence: 4 givenname: Ewa surname: Krzyżyńska-Malinowska fullname: Krzyżyńska-Malinowska, Ewa organization: Biology, Ludwik Rydygier Medical University, Bydgoszcz, Poland |
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Keywords | Human Skin disease Sporadic Check Malignant tumor Review Carcinogenesis G1 Phase Regulation(control) C-Onc gene Cell cycle Malignant melanoma Skin Molecular biology Protooncogene Tumor suppressor gene |
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References_xml | – reference: Israels ED, Israels LG. The cell cycle. Oncologist 2000; 5: 510-513. – reference: Keller-Melchior R, Schmidt R, Piepkorn M. Expression of the tumor suppressor gene product p16INK4 in benign and malignant melanocytic lesions. J Invest Dermatol 1998; 110: 932-938. – reference: Akslen LA, Monstad SE, Larsen B, et al. Frequent mutations of the p53 gene in cutaneous melanoma of the nodular type. Int J Cancer 1998; 79: 91-95. – reference: Bartek J, Lukas J, Bartkova J. Perspective: defects in cell cycle control and cancer. J Pathol 1999; 187: 95-99. – reference: Kumar R, Sauroja I, Punnonen K, et al. Selective deletion of exon 1β of the p19ARF gene in metastatic melanoma cell lines. Genes Chromosomes Cancer 1998; 23: 273-277. – reference: Fujimoto A, Morita R, Hatta N, et al. p16INK4a inactivation is not frequent in uncultured sporadic primary cutaneous melanoma. 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Snippet | Sporadic melanoma is a neoplasm whose etiology has not been fully investigated. Contemporary achievements in molecular biology have made it possible to... |
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SubjectTerms | Biological and medical sciences Cell Cycle - genetics Cell Cycle - physiology Dermatology G1 Phase - genetics G1 Phase - physiology Genes, cdc - physiology Humans Medical sciences Melanoma - genetics Melanoma - physiopathology Skin Neoplasms - genetics Skin Neoplasms - physiopathology Tumors of the skin and soft tissue. Premalignant lesions |
Title | Cell cycle in sporadic melanoma |
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