UNLABELLED: To screen and analyze the apoptosis- and proliferation-related genes in human nasopharyngeal carcinoma (NPC). METHODS: According to gene ontology classification, the abnormal expressions of the genes related to cell apoptosis and proliferation were identified in the NPC gene chip data. The cell apoptosis- and proliferation-related genes expressed in each of the 3 stages, as defined by the tree model for the pathogenesis and progression of NPC, were screened, and with literature review, their distribution in the tree model were analyzed. RESULTS: Nineteen genes related to cell apoptosis were found in NPC, among which 9 were down-regulated (such as DNASE1L3) and located in the chromosome deletion regions, and 10 were up-regulated (such as DEDD) in the chromosome amplification regions. Twenty-one cell proliferation-related genes were identified, including 8 down-regulated genes (such as TUSC2) in the chromosome deletion regions and 13 up-regulated ones (such as EMP1) in the chromosome amplification regions. In the chromosome deletion regions, the down-regulated cell apoptosis-related genes participated mostly in inducing and regulating cell apoptosis, and the up-regulated cell proliferation-related genes in the chromosome amplification regions were mostly associated with the positive regulation of cell proliferation. CONCLUSION: NPC occurs possibly through two pathways by inhibiting cell apoptosis or by promoting excessive cell proliferation.
UNLABELLED: To screen and analyze the apoptosis- and proliferation-related genes in humannasopharyngeal carcinoma (NPC). METHODS: According to gene ontology classification, the abnormal expressions of the genes related to cell apoptosis and proliferation were identified in the NPC gene chip data. The cell apoptosis- and proliferation-related genes expressed in each of the 3 stages, as defined by the tree model for the pathogenesis and progression of NPC, were screened, and with literature review, their distribution in the tree model were analyzed. RESULTS: Nineteen genes related to cell apoptosis were found in NPC, among which 9 were down-regulated (such as DNASE1L3) and located in the chromosome deletion regions, and 10 were up-regulated (such as DEDD) in the chromosome amplification regions. Twenty-one cell proliferation-related genes were identified, including 8 down-regulated genes (such as TUSC2) in the chromosome deletion regions and 13 up-regulated ones (such as EMP1) in the chromosome amplification regions. In the chromosome deletion regions, the down-regulated cell apoptosis-related genes participated mostly in inducing and regulating cell apoptosis, and the up-regulated cell proliferation-related genes in the chromosome amplification regions were mostly associated with the positive regulation of cell proliferation. CONCLUSION: NPC occurs possibly through two pathways by inhibiting cell apoptosis or by promoting excessive cell proliferation.
Authors: Jaroslaw Szczyrba; Volker Jung; Michaela Beitzinger; Elke Nolte; Sven Wach; Martin Hart; Sandra Sapich; Marc Wiesehöfer; Helge Taubert; Gunther Wennemuth; Norbert Eichner; Thomas Stempfl; Bernd Wullich; Gunter Meister; Friedrich A Grässer Journal: Prostate Cancer Date: 2017-01-05
Authors: Semra Demokan; Alice Y Chuang; Xiaofei Chang; Tanbir Khan; Ian M Smith; Kavita M Pattani; Santanu Dasgupta; Shahnaz Begum; Zubair Khan; Nanette J Liegeois; William H Westra; David Sidransky; Wayne Koch; Joseph A Califano Journal: Int J Oncol Date: 2013-02-06 Impact factor: 5.650