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Encyclopedia results for Oncogenesis

Oncogenesis





Encyclopedia results for Oncogenesis

  1. Critical Reviews in Oncogenesis

    Italic title Critical Reviews in Oncogenesis ISSN 0893 9675 is a quarterly scientific journal published by Begell House covering the field of oncology . The editor in chief is Ragnhild A. Lothe . External links Official http www.begellhouse.com journals 439f422d0783386a Category Oncology journals Category Quarterly journals Category English language journals Category Begell House academic journals ...   more details



  1. Activating transcription factor

    In molecular biology , activating transcription factor , ATF , is a class of AP 1 transcription factor AP 1 transcription factor dimers. ref name van Dam cite journal author van Dam H, Castellazzi M title Distinct roles of Jun Fos and Jun ATF dimers in oncogenesis journal Oncogene volume 20 issue 19 pages 2453 64 year 2001 pmid 11402340 doi 10.1038 sj.onc.1204239 ref Genes include ATF1 , Activating transcription factor 2 ATF2 , ATF3 , ATF4 , ATF5 , ATF6 , and ATF7 . References references External links MeshName Activating Transcription Factors protein stub Oncogenes Transcription factors g1 Category Transcription factors es Factor de transcripci n activador ...   more details



  1. Mitotic catastrophe

    orphan date October 2009 Mitotic catastrophe is an event in which a cell is destroyed during mitosis . Cells which fail to go through a mitotic catastrophe after a mitotic failure are likely to create aneuploidy aneuploid cells when they later reproduce, posing a risk of oncogenesis , potentially leading to cancer. External links cite journal author Castedo M, Perfettini JL, Roumier T, Andreau K, Medema R, Kroemer G. date 12 April 2004 title Cell death by mitotic catastrophe a molecular definition journal Oncogene journal Oncogene volume 23 issue 16 pages 2825 2837 issn 0950 9232 doi 10.1038 sj.onc.1207528 pmid 15077146 url http www.nature.com onc journal v23 n16 abs 1207528a.html Category Apoptosis Category Cell cycle Category Mitosis Category Programmed cell death ...   more details



  1. The Diamantina Institute for Cancer, Immunology and Metabolic Medicine

    in the molecular oncogenesis group focus on the molecular regulation of cell proliferation and differentiation ...   more details



  1. Origin recognition complex

    Refimprove date December 2009 Image CDC6 Function.jpg thumb Potential role of Cdc6 at the initiation of DNA replication. ref name pmid18048387 cite journal author Borlado LR, M ndez J title CDC6 from DNA replication to cell cycle checkpoints and oncogenesis journal Carcinogenesis volume 29 issue 2 pages 237 43 year 2008 month February pmid 18048387 doi 10.1093 carcin bgm268 url issn ref ORC or Origin Recognition Complex is a multi subunit ref MeshName Origin Recognition Complex ref DNA binding complex 6 subunits that binds in all eukaryotes in an ATP dependent manner to origins of replication . During the G1 phase of the cell cycle, when S phase Cyclin dependent kinase CDK levels are low, ORC recruits Cdc6 and Cdt1. One Cdc6 and one Cdt1 bind to each strand of DNA. Cdc6 and Cdt1 interact with each other and inhibit Mini Chromosome Maintenance Mcm , a DNA helicase that binds after Cdc6 and Cdt1 binding to the ORC. The ORC, Cdc6 , Cdt1 and Mini Chromosome Maintenance Mcm proteins form the Pre replication complex . Activated S CDK triggers S phase and phosphorylates Cdc6 . Phosphorylated Cdc6 is degraded. Cdt1 is inhibited by geminin . With Cdc6 and Cdt1 no longer bound, Mini Chromosome Maintenance Mcm can unwind the double stranded DNA allowing the preinitiation complex to bind. ORC is phosphorylated and DNA replication takes place. DDK also participates in ORC activation and triggers the transition into DNA replication. References Reflist DNA replication DEFAULTSORT Origin Recognition Complex Category Eukaryotes Category DNA Genetics stub es Complejo de reconocimiento de origen it Origin Recognition Complex ...   more details



  1. Metallopanstimulin

    Orphan date February 2009 Metallopanstimulin or MPS is a zinc finger protein proposed to be involved DNA repair as well as oncogenesis . ref Fernandez Pol JA. Metallopanstimulin as a novel tumor marker in sera of patients with various types of common cancers implications for prevention and therapy Anticancer Research 1996 Jul Aug 16, pp. 2177 85. ref Its expression is increased in several types of malignancy and MPS levels have been reported to drop with treatment of some cancer s. It has also been used as a target for some chemotherapy chemotherapies , which aim to chelation chelate out the zinc from the zinc finger motif of the MPS, thus yielding it inactive. These therapies have shown promise for the treatment of cancer in laboratory experiments and some limited clinical trial s. Head and neck cancer transfected to overexpress this protein have demonstrated suppressed growth. References references cite journal author Scurry WC Jr, Stack BC Jr. title Role of metalloproteins in the clinical management of head and neck squamous cell carcinoma journal Head Neck year 2007 month December volume 29 issue 12 pages 1144 55 pmid 17657798 doi 10.1002 hed.20655 cite journal author Stack BC Jr, Hollenbeak CS, Lee CM, Dunphy FR, Lowe VJ, Hamilton PD title Metallopanstimulin as a marker for head and neck cancer journal World J Surg Oncol year 2004 month December volume 14 pages 2 45 pmid 15598348 doi 10.1186 1477 7819 2 45 pmc 544581 cite journal author Lee WJ, Keefer K, Hollenbeak CS, Stack BC Jr. title A new assay to screen for head and neck squamous cell carcinoma using the tumor marker metallopanstimulin journal Otolaryngol Head Neck Surg year 2004 month October volume 131 issue 4 pages 466 71 pmid 15467619 doi 10.1016 j.otohns.2004.03.011 Category Proteins protein stub ...   more details



  1. WNT6

    protein Name wingless type MMTV integration site family, member 6 caption image width HGNCid 12785 Symbol WNT6 AltSymbols EntrezGene 7475 OMIM 604663 RefSeq NM 006522 UniProt Q9Y6F9 PDB ECnumber Chromosome 2 Arm q Band 35 LocusSupplementaryData Wingless type MMTV integration site family, member 6 , also known as WNT6 , is a human gene . ref name entrez cite web title Entrez Gene WNT2 wingless type MMTV integration site family, member 2 url http www.ncbi.nlm.nih.gov sites entrez?Db gene&Cmd ShowDetailView&TermToSearch 7475 accessdate ref ref name pmid10343101 cite journal author Rankin J, Strachan T, Lako M, Lindsay S title Partial cloning and assignment of WNT6 to human chromosome band 2q35 by in situ hybridization journal Cytogenet. Cell Genet. volume 84 issue 1 2 pages 50 2 year 1999 pmid 10343101 doi 10.1159 000015212 url ref The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family which are involved in the Wnt signaling pathway . It is overexpressed in cervical cancer cell line and strongly coexpressed with another family member, WNT10A , in colorectal cancer cell line. ref name pmid11350055 cite journal author Kirikoshi H, Sekihara H, Katoh M title WNT10A and WNT6, clustered in human chromosome 2q35 region with head to tail manner, are strongly coexpressed in SW480 cells journal Biochem. Biophys. Res. Commun. volume 283 issue 4 pages 798 805 year 2001 month May pmid 11350055 doi 10.1006 bbrc.2001.4855 url ref The gene overexpression may play key roles in carcinogenesis. This gene and the WNT10A gene are clustered in the chromosome 2q35 region. The protein encoded by this gene is 97 identical to the mouse Wnt6 protein at the amino acid level. ref name entrez References reflist gene 2 stub NLM content ...   more details



  1. ZNF703

    Wikify date February 2011 Orphan date February 2011 protein name zinc finger protein 703 caption image width HGNCid 25883 Symbol ZNF703 AltSymbols EntrezGene 80139 OMIM RefSeq NM 025069 UniProt PDB ECnumber Chromosome 8 Arm p Band 12 LocusSupplementaryData ZNF703 is a gene. ref name pmid21328542 cite journal author Sircoulomb F, Nicolas N, Ferrari A, et al. title ZNF703 gene amplification at 8p12 specifies luminal B breast cancer journal EMBO Mol Med volume issue pages year 2011 month February pmid 21328542 doi 10.1002 emmm.201100121 url ref ref name pmid19330026 cite journal author Kwek SS, Roy R, Zhou H, et al. title Co amplified genes at 8p12 and 11q13 in breast tumors cooperate with two major pathways in oncogenesis journal Oncogene volume 28 issue 17 pages 1892 903 year 2009 month April pmid 19330026 pmc 2722962 doi 10.1038 onc.2009.34 url http dx.doi.org 10.1038 onc.2009.34 ref It is an oncogene . ref name urlBBC News Key breast cancer driver gene found cite web url http www.bbc.co.uk news health 12503798 title BBC News Key breast cancer driver gene found format work accessdate 2011 02 18 ref References reflist Genetics stub ...   more details



  1. Mammalian promoter database

    Wikify date April 2011 Orphan date March 2011 infobox biodatabase title MPromDb logo File Database.png description annotation and visualization of mammalian gene promoters and ChIP seq experimental data. scope organism center laboratory Center for Systems and Computational Biology, Molecular and Cellular Oncogenesis Program, The Wistar Institute, Philadelphia, PA, USA. author Ravi Gupta pmid Gupta & al. 2011 ref name pmid21097880 released 2010 standard format url http bioinformatics.wistar.upenn.edu MPromDb download webservice sql sparql webapp standalone license versioning frequency curation bookmark version MPromDb Mammalian Promoter Database is a curated database of gene Promoter biology promoter s identified from Chip Sequencing ChIP seq ref name pmid21097880 cite journal quotes yes last Gupta first Ravi authorlink coauthors Bhattacharyya Anirban, Agosto Perez Francisco J, Wickramasinghe Priyankara, Davuluri Ramana V year 2011 month Jan title MPromDb update 2010 an integrated resource for annotation and visualization of mammalian gene promoters and ChIP seq experimental data journal Nucleic Acids Res. volume 39 issue Database issue pages D92 7 publisher location England issn pmid 21097880 doi 10.1093 nar gkq1171 bibcode oclc id url pmc 3013732 language eng format accessdate laysummary laysource laydate quote ref References references External links http bioinformatics.wistar.upenn.edu MPromDb Category Biological databases Category Gene expression Category Protein methods Biodatabase stub ...   more details



  1. Caveolae

    In biology , caveolae Latin for little caves , singular caveola , which are a special type of lipid raft , are small 50 100 nanometer invagination s of the plasma membrane in many vertebrate cell biology cell types, especially in endothelium endothelial cells and adipocyte s. These flask shaped structures are rich in protein s as well as lipid s such as cholesterol and sphingolipid s and have several functions in signal transduction . ref cite journal author Anderson RG title The caveolae membrane system journal Annu. Rev. Biochem. volume 67 issue pages 199 225 year 1998 pmid 9759488 doi 10.1146 annurev.biochem.67.1.199 url http arjournals.annualreviews.org doi abs 10.1146 annurev.biochem.67.1.199?url ver Z39.88 2003&rfr id ori rid crossref.org&rfr dat cr pub 3dncbi.nlm.nih.gov ref They are also believed to play a role in endocytosis , oncogenesis , and the uptake of pathogen ic bacteria and certain virus es. ref cite journal author Frank P, Lisanti M title Caveolin 1 and caveolae in atherosclerosis differential roles in fatty streak formation and neointimal hyperplasia. journal Curr Opin Lipidol volume 15 issue 5 pages 523 9 year 2004 pmid 15361787 doi 10.1097 00041433 200410000 00005 ref ref cite journal author Li X, Everson W, Smart E title Caveolae, lipid rafts, and vascular disease. journal Trends Cardiovasc Med volume 15 issue 3 pages 92 6 year 2005 pmid 16039968 doi 10.1016 j.tcm.2005.04.001 ref ref cite journal author Pelkmans L title Secrets of caveolae and lipid raft mediated endocytosis revealed by mammalian viruses. journal Biochim Biophys Acta volume 1746 issue 3 pages 295 304 year 2005 pmid 16126288 doi 10.1016 j.bbamcr.2005.06.009 ref Caveolae are one source of clathrin independent endocytosis involved in turnover of adhesive complexes. Formation and maintenance of caveolae is primarily due to the protein caveolin , ref MeshName Caveolae ref a 21 kD protein. This protein has both a cytoplasm ic C terminus and a cytoplasmic N terminus, linked together ...   more details



  1. LIM domain

    Pfam box Symbol LIM Name LIM domain image Lims.png width 200 caption Structure of the 4th LIM domain of Pinch protein. Zinc atoms are shown in grey Pfam PF00412 InterPro IPR001781 SMART PROSITE PDOC50178 SCOP 1ctl TCDB OPM family OPM protein PDB PDB3 1ctl A 11 67 LIM domains are protein structural domain s, composed of two contiguous zinc finger domains, separated by a two amino acid residue hydrophobic linker. ref name pmid15520811 cite journal author Kadrmas JL, Beckerle MC title The LIM domain from the cytoskeleton to the nucleus journal Nat. Rev. Mol. Cell Biol. volume 5 issue 11 pages 920 31 year 2004 pmid 15520811 doi 10.1038 nrm1499 issn ref They are named after their initial discovery in the proteins L in11, I sl 1 & M ec 3. ref name pmid10704826 cite journal author Bach I title The LIM domain regulation by association journal Mech. Dev. volume 91 issue 1 2 pages 5 17 year 2000 pmid 10704826 doi 10.1016 S0925 4773 99 00314 7 issn ref LIM domain containing proteins have been shown to play roles in cytoskeleton cytoskeletal organisation, organ development and oncogenesis . LIM domains mediate protein protein interactions protein protein interactions that are critical to cellular processes. LIM domains have highly divergent sequences, apart from certain key residues. The sequence divergence allow a great many different binding sites to be grafted onto the same basic domain. The conserved residues are those involved in zinc binding or the hydrophobic core of the protein. The sequence signature of LIM domains is as follows C X sub 2 4 sub C X sub 13 19 sub W H X sub 2 4 sub C F LVI C X sub 2 4 sub C X sub 13 20 sub C X sub 2 4 sub C Image Lim diag.png thumb 200px Lim domain organsiation LIM domains frequently occur in multiples, as seen in proteins such as TES protein TES , LMO4, and can also be attached to other domains in order to confer a binding or targeting function upon them, such as LIM kinase. References div class references small style moz column count 2 ...   more details



  1. Rhesus lymphocryptovirus

    Taxobox color violet name Rhesus Lymphocryptovirus virus group i familia Herpesviridae subfamilia Gammaherpesvirinae genus Lymphocryptovirus species Rhesus Lymphocryptovirus The rhesus lymphocryptovirus rhesus LCV, RLV, Cercopithecine HV 15 is a lymphocryptovirus gamma 1 herpesvirus in the same genus as the Epstein Barr virus EBV . Its genetics genetic structure has been fully sequenced and found to be highly homologous with that of EBV 65 . The structural proteins are highly conserved, while genes expressed during EBV latent infection are much less well conserved. Even in cases where genes have low Homology biology homology , the rLCV infection genes are functionally interchangeable with EBV genes. In nature, RLV infects rhesus macaques . ref cite journal author Rivailler P, Jiang H, Cho YG, Quink C, Wang F title Complete nucleotide sequence of the rhesus lymphocryptovirus genetic validation for an Epstein Barr virus animal model journal J Virol. 2002 Jan 76 1 421 6 volume 1976 12 3 4 163 8 pmid 11739708 doi year 2002 issue 1 pages 421 6 pmc 135707 ref RLV infection in rhesus monkeys resembles EBV infection in humans in several respects oral transmission, atypical lymphocytosis , lymphadenopathy , activation of CD23 peripheral blood B cells , sustained serologic responses to lytic and Virus latency latent EBV antigens , latent infection in the peripheral blood, and virus persistence in oropharyngeal secretions. These features make the rhesus lymphocryptovirus potentially useful for studying the pathogenesis , prevention, and treatment of EBV infection and associated oncogenesis . ref cite journal journal Science volume 27 June 1997 Vol. 276. no. 5321, pp. 2030 2033 title An Animal Model for Acute and Persistent Epstein Barr Virus Infection author Amir Moghaddam, Michael Rosenzweig, David Lee Parritz, Bethany Annis, R. Paul Johnson, Fred Wang url http www.sciencemag.org cgi content abstract 276 5321 2030?ck nck pmid 9197263 doi 10.1126 science.276.5321.2030 year 199 ...   more details



  1. Jaagsiekte

    pubmed docsum Transformation and oncogenesis by jaagsiekte sheep retrovirus. http jnci.oxfordjournals.org ...   more details



  1. Pin1

    distinguish2 PIN1 Pin formed 1 , an auxin transporter in Arabidopsis thaliana Orphan date February 2009 Pin 1 , or peptidyl prolyl cis trans isomerase PPIase , isomerizes only phospho Serine Threonine Proline sequence motif motifs . The enzyme binds to a subset of proteins and thus plays a role as a post phosphorylation control in regulating protein function. Studies have shown that the deregulation of Pin1 may play a pivotal role in various diseases. Notably, the up regulation of Pin1 may be implicated in certain cancers , and the down regulation of Pin1 may be implicated in Alzheimer s disease . Inhibitors of Pin1 may have therapeutic implications for cancer and immune disorders . Discovery and characterization The gene encoding Pin1 was identified in 1996 as a result of a genetic biochemical screen for proteins involved in mitotic regulation . It was found to be essential for cell division in some organisms. By 1999, however, it was apparent that Pin1 knockout mice had a surprisingly mild phenotype , indicating that the enzyme was not required for cell division per se. Further studies later found that loss of Pin1 in mice displays not only neuronal degenerative phenotypes but also several abnormalities, similar to those of cyclin D1 null mice, suggesting the conformation changes mediated by Pin1 may be crucial for cell normal function. Activation of Pin1 Phosphorylation of Ser Thr Pro motifs in substrates is required for recognition by Pin1. Pin is a small protein at 18 kDa and does not have a nuclear localization or export signal. Substrate interactions and a WW domain determine subcellular distribution. Expression is induced by growth signals from E2F transcription factors. Expression levels fluctuate in normal, but not in cancerous cells. Expression is often associated with cell proliferation . Postranslational modifications such as phosphorylation on Ser16 inhibit the ability of Pin1 to bind substrate, and this inhibitory process may be altered during oncogen ...   more details



  1. Lysophosphatidic acid

    chembox verifiedrevid 403301425 ImageFile Lysophosphatidic acid.svg ImageSize 250px IUPACName 2 hydroxy 3 phosphonooxypropyl Z octadec 9 enoate OtherNames LPA Section1 Chembox Identifiers CASNo 22002 87 5 PubChem 5497152 SMILES CCCCCCCC C C CCCCCCCC O OCC COP O O O O MeSHName lysophosphatidic acid Section2 Chembox Properties Formula C sub 21 sub H sub 41 sub O sub 7 sub P MolarMass 436.52 g mol Appearance Density MeltingPt BoilingPt Section3 Chembox Hazards Solubility MainHazards FlashPt Autoignition Lysophosphatidic acid LPA is a phospholipid derivative that can act as a lipid signaling signaling molecule. ref name GarrettGrisham2008 cite book author1 Reginald Garrett author2 Charles M. Grisham title Biochemistry url http books.google.com books?id iGPsen3fSOIC&pg PA235 accessdate 20 December 2010 date 28 December 2008 publisher Cengage Learning isbn 9780495109358 pages 235 ref Function LPA acts as a potent mitogen due to its activation of three high affinity G protein coupled receptors called Lysophospholipid receptor LPA1 , Lysophospholipid receptor LPA2 , and Lysophospholipid receptor LPA3 also known as EDG2, EDG4, and EDG7 . Additional, newly identified LPA receptors include LPA4 p2y9 GPR23 , LPA5 GPR92 and LPA6 GPR87 . Clinical significance Because of its ability to stimulate cell proliferation , aberrant LPA signaling has been linked to cancer in numerous ways. Dysregulation of autotaxin or the LPA receptors can lead to hyperproliferation, which may contribute to oncogenesis and metastasis . LPA may be the cause pruritus itching in individuals with cholestatic impaired bile flow diseases. GTPase activation Downstream of LPA receptor activation, the small GTPase Rho can be activated, subsequently activating Rho kinase. This can lead to the formation of stress fibers and cell migration through the inhibition of myosin light chain phosphatase . Metabolism There are a number of potential routes to its biosynthesis, but the most well characterized is by the action ...   more details



  1. Herbimycin

    in the regulation of the cell cycle, cell growth, cell survival, apoptosis , angiogenesis and oncogenesis ...   more details



  1. Radicicol

    and oncogenesis . Further reading cite journal author Winssinger N, Barluanga S title Chemistry and biology ...   more details



  1. Minichromosome maintenance

    Pfam box Symbol MCM Name MCM2 3 5 family image PDB 1ltl EBI.jpg width caption Structure of MCM from archaeal M. Thermoautotrophicum . ref name pmid12548282 cite journal author Fletcher RJ, Bishop BE, Leon RP, Sclafani RA, Ogata CM, Chen XS title The structure and function of MCM from archaeal M. Thermoautotrophicum journal Nat. Struct. Biol. volume 10 issue 3 pages 160 7 year 2003 month March pmid 12548282 doi 10.1038 nsb893 url ref Pfam PF00493 Pfam clan CL0023 InterPro IPR001208 SMART SM00350 PROSITE PDOC00662 SCOP TCDB OPM family OPM protein PDB PDB2 1ltl Image CDC6 Function.jpg thumb Potential role of Cdc6 at the initiation of DNA replication. ref name pmid18048387 cite journal author Borlado LR, M ndez J title CDC6 from DNA replication to cell cycle checkpoints and oncogenesis journal Carcinogenesis volume 29 issue 2 pages 237 43 year 2008 month February pmid 18048387 doi 10.1093 carcin bgm268 url issn ref Mini Chromosome Maintenance complex , or Minichromosome Maintenance protein complex or mini chromosome maintenance MCM 2 7 helicase complex has a role in both the initiation and the elongation phases of eukaryotic DNA replication , specifically the formation and elongation of the replication fork . MCM is a component of the pre replication complex , which is a component of the licensing factor . MCM is a hexamer of six related polypeptides mcm2 7 that form a ring structure. ref name pmid15210935 cite journal author Cortez D, Glick G, Elledge SJ title Minichromosome maintenance proteins are direct targets of the ATM and ATR checkpoint kinases journal Proc. Natl. Acad. Sci. U.S.A. volume 101 issue 27 pages 10078 83 year 2004 month July pmid 15210935 pmc 454167 doi 10.1073 pnas.0403410101 url issn ref ref name pmid11821426 cite journal author Carpentieri F, De Felice M, De Falco M, Rossi M, Pisani FM title Physical and functional interaction between the mini chromosome maintenance like DNA helicase and the single stranded DNA binding protein from the crenarchaeo ...   more details



  1. Genetics of cancer

    orphan date June 2009 Cancer is a Genetics genetic Genetic disorder disorder in which the normal control of cell growth is lost. Cancer genetics is now one of the fastest expanding Specialty medicine medical specialties . At the Molecule molecular level, cancer is caused by Mutation mutation s in DNA , which result in aberrant Cell biology cell proliferation. Most of these mutations are Mutagen acquired and occur in somatic cell s. However, some people Heredity inherit mutation s in the germline . ref Fiona Lalloo. Genetics of Oncologists. ISBN.1901346196. remedica Publishing ref The mutation s occur in two classes of cellular gene s oncogene s and tumor suppressor gene s . Oncogene main Oncogene Oncogenes are derived from normal cellular genes called Oncogene Proto oncogene proto oncogenes . Proto oncogenes were first elucidated in RNA tumor virus es and are now known to Genetic code encode protein s that are crucial for cellular growth regulation e.g. growth factor, Signal transduction Cell surface receptors cell surface receptors , DNA Carrier protein binding proteins , etc. Mutation in cancer cells alter the normal structure and or expression pattern of the proto oncogene, generating Oncogenesis oncogenic variant forms with altered function. In genetic terms, oncogenic allele s have gain of function mutation . Transformation of proto oncogene to oncogene ref Robert F. Mueller AND Young I.D.Emery s Elements of Medical Genetics. ISBN.0 443 07125 X ref is the result of gain in function through Over Gene expression expression of the gene, or Gene duplication duplication such as Gene duplication Gene duplication as amplification amplification to produce increased onco protein Activation Biochemistry Activation or formation of fusion gene by Chromosomal translocation translocation Alteration of the gene product to produce Transformation genetics transforming proteins Examples of Oncogenes Signal transduction protein s Abl gene Abl Src gene Src H ras N ras Cell nucleus ...   more details



  1. NUP88

    , Silver PA title Diverse nuclear transport pathways regulate cell proliferation and oncogenesis. journal ... in oncogenesis and development. journal Am. J. Pathol. volume 157 issue 5 pages 1605 13 year 2000 ...   more details



  1. Epstein-Barr nuclear antigen 1

    EBNA1 is a well characterized protein, its role in oncogenesis is less well defined. It is consistently ... author Young, Lawrence S., Paul G. Murry title Epstein Barr Virus and oncogenesis from latent ...   more details



  1. Geldanamycin

    of the cell cycle, cell growth, cell survival, apoptosis , angiogenesis and oncogenesis ...   more details



  1. Rous sarcoma virus

    Taxobox Color parameter is not needed automatically assigned name Rous sarcoma virus virus group vi familia Retroviridae subfamilia Orthoretrovirinae genus Alpharetrovirus species Rous sarcoma virus Rous sarcoma virus is a retrovirus and is the first oncovirus to have been described it causes sarcoma in chickens. As with all retroviruses, it reverse transcribes its RNA genome into cDNA before integration into the host DNA. History RSV was discovered in 1911 by Peyton Rous , working at Rockefeller University in New York City, by injecting cell free extract of chicken tumour into healthy Plymouth Rock chickens. The extract was found to induce oncogenesis . The tumour was found to be composed of connective tissue a sarcoma . Rous was awarded the Nobel Prize for the significance of his discovery in 1966 . Structure and genome RSV is a class VI enveloped virus with a positive sense RNA genome having a DNA intermediate. RSV has three genes gag gene gag encodes capsid proteins pol gene pol encodes reverse transcriptase It lost the env gene normally seen in avian retroviruses during the recombination events that allowed it to acquire src src gene src encodes a tyrosine kinase that attaches phosphate groups to the amino acid tyrosine in host cell proteins. The RSV genome has terminal repeat s enabling its integration into the host genome and also overexpression of RSV genes. src gene The Src gene src gene is oncogene oncogenic as it triggers uncontrolled growth in abnormal host cells. It is an acquired gene, found to be present throughout the animal kingdom with high levels of conservation between species. The src gene was taken up by RSV and incorporated into its genome conferring it with the advantage of being able to stimulate uncontrolled mitosis of host cells, providing abundant cells for fresh infection . The src gene is not essential for RSV proliferation but it greatly increases virulence when present. RNA secondary structure Image RSV secondary structure.jpg thumb 2 ...   more details



  1. Small nucleolar RNA SNORD50

    paralogues form a novel family of genes controlling oncogenesis and sensitivity to therapy in cancer ...   more details



  1. Feline sarcoma oncogene

    in oncogenesis volume 9 issue 1 pages 43 62 year 1998 pmid 9754447 doi cite journal author Jiang ...   more details




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