癌基因抑癌基因与生长因子讲稿.ppt

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1、关于癌基因抑癌基因与生长因子第一页，讲稿共一百五十五页哦 细胞的正常生长与增殖由两大类基因调控：细胞的正常生长与增殖由两大类基因调控：正调节信号正调节信号 促进细胞生长和增殖，并阻止其促进细胞生长和增殖，并阻止其发生终末分化。发生终末分化。负调控信号负调控信号 抑制增殖抑制增殖,促进分化、成熟和衰促进分化、成熟和衰老，最后凋亡。老，最后凋亡。这两类基因中任何一种或它们共同的变化，即这两类基因中任何一种或它们共同的变化，即有可能引起细胞增殖失控导致肿瘤的发生有可能引起细胞增殖失控导致肿瘤的发生。第二页，讲稿共一百五十五页哦癌基因与抑癌基因的作用机制涉及基因表癌基因与抑癌基因的作用机制涉及基因表达

2、调控及细胞分裂、分化。达调控及细胞分裂、分化。癌基因可编码类生长因子多肽及其受体分癌基因可编码类生长因子多肽及其受体分子，通过细胞内信息传递系统刺激细胞增子，通过细胞内信息传递系统刺激细胞增殖。殖。肿瘤的发生与癌基因、抑癌基因和生长因肿瘤的发生与癌基因、抑癌基因和生长因子三者的关系密切相关。子三者的关系密切相关。第三页，讲稿共一百五十五页哦第一节 癌基因第四页，讲稿共一百五十五页哦l癌基因（癌基因（oncogeneoncogene）就是具有增加癌源性或转化潜能，）就是具有增加癌源性或转化潜能，导致其编码区或调节区域遗传性状发生改变的基因。导致其编码区或调节区域遗传性状发生改变的基因。l癌基因可

3、分为两大类：一类是致瘤病毒中能在体内癌基因可分为两大类：一类是致瘤病毒中能在体内诱发肿瘤并在体外引起细胞转化的基因，即病毒癌诱发肿瘤并在体外引起细胞转化的基因，即病毒癌基因（基因（viral oncogene,v-oncviral oncogene,v-onc）；另一类是存在于细）；另一类是存在于细胞基因组中、正常情况下处于静止或低水平（限制性）胞基因组中、正常情况下处于静止或低水平（限制性）表达状态，对维持细胞正常功能具有重要作用，当受到表达状态，对维持细胞正常功能具有重要作用，当受到致癌因素作用被活化而导致细胞恶变的基因，即原癌基致癌因素作用被活化而导致细胞恶变的基因，即原癌基因（因（pr

4、otooncogeneprotooncogene，pro-oncpro-onc）或称细胞癌基因）或称细胞癌基因（cellular oncogenecellular oncogene，c-oncc-onc）。）。一、病毒癌基因和细胞癌基因 （一）概念第五页，讲稿共一百五十五页哦 癌癌基基因因名名称称用用3 3个个斜斜体体小小写写字字母母表表示示，如如mycmyc、rasras、srcsrc。l肿瘤病毒是一类能使宿主产生肿瘤或使培养细肿瘤病毒是一类能使宿主产生肿瘤或使培养细胞转化成癌细胞的动物病毒。胞转化成癌细胞的动物病毒。l其核酸组成分为其核酸组成分为DNADNA病毒病毒和和RNARNA病毒病毒

5、。l病毒癌基因病毒癌基因是一类存在于肿瘤病毒（大多数是是一类存在于肿瘤病毒（大多数是逆转录病毒）中的、能使靶细胞发生恶性转化逆转录病毒）中的、能使靶细胞发生恶性转化的基因。的基因。第六页，讲稿共一百五十五页哦 l19111911年，年，Reyton Rous Reyton Rous 报道将鸡肉瘤的无细胞滤液注报道将鸡肉瘤的无细胞滤液注射给健康鸡后，可诱导发生肉瘤，表明无细胞滤液射给健康鸡后，可诱导发生肉瘤，表明无细胞滤液含致含致病原，可传播肿瘤。病原，可传播肿瘤。l19321932年，年，ShopeShope发现，野生棉尾兔的皮肤肿瘤也可借助发现，野生棉尾兔的皮肤肿瘤也可借助无细胞滤液传播。无

6、细胞滤液传播。l肿瘤进展：肿瘤进展：开始，癌细胞处于开始，癌细胞处于“休眠休眠”状态，被化学状态，被化学因子、病毒等唤醒后，变的无法无天。因子、病毒等唤醒后，变的无法无天。lRousRous提出病毒致癌理论：提出病毒致癌理论：即传播肿瘤的无细胞滤液中即传播肿瘤的无细胞滤液中含的是病毒。含的是病毒。l这种感染性颗粒后来被证实是逆转录病毒这种感染性颗粒后来被证实是逆转录病毒(RNA(RNA病毒病毒)。RousRous因此获得因此获得19661966年诺贝尔生理和医学奖。年诺贝尔生理和医学奖。癌基因的发现第七页，讲稿共一百五十五页哦The Nobel Prize in Physiology or M

7、edicine 1966 Tumor-inducing viruses第八页，讲稿共一百五十五页哦Peyton RousUSARockefeller UniversityNew York,NY,USAB:1879D:1970第九页，讲稿共一百五十五页哦鸡肉瘤病毒（鸡肉瘤病毒（RSV)RSV)基因组结构图基因组结构图 病毒癌基因与正常细胞中的原癌基因同源病毒癌基因与正常细胞中的原癌基因同源第十页，讲稿共一百五十五页哦 病病毒毒癌癌基基因因致致癌癌机机制制第十一页，讲稿共一百五十五页哦l l19641964年年年年H.M.TeminH.M.TeminH.M.TeminH.M.Temin认为，认为，

8、RSVRSVRSVRSV的生活周期中存在着的生活周期中存在着的生活周期中存在着的生活周期中存在着前病前病前病前病毒毒毒毒（provirusprovirus）的）的）的）的DNADNA中间产物阶段，中间产物阶段，中间产物阶段，中间产物阶段，DNADNADNADNA前病毒含有前病毒含有前病毒含有前病毒含有RNARNA病毒基因组的全部信息。病毒基因组的全部信息。病毒基因组的全部信息。病毒基因组的全部信息。l l子代病毒子代病毒RNARNARNARNA是以前病毒是以前病毒是以前病毒是以前病毒DNADNA为模版合成的。前病毒可整为模版合成的。前病毒可整为模版合成的。前病毒可整为模版合成的。前病毒可整合到

9、宿主细胞基因组中。通过病毒的诱导，正常细胞可合到宿主细胞基因组中。通过病毒的诱导，正常细胞可合到宿主细胞基因组中。通过病毒的诱导，正常细胞可合到宿主细胞基因组中。通过病毒的诱导，正常细胞可转化转化转化转化成肿瘤细胞。成肿瘤细胞。成肿瘤细胞。成肿瘤细胞。l l1970197019701970年年年年TeminTeminTeminTemin实验室和实验室和实验室和实验室和Baltimove Baltimove 实验室分别发现实验室分别发现RSVRSVRSVRSV病毒粒子中含有病毒粒子中含有反转录酶反转录酶反转录酶反转录酶。这一结果使。这一结果使。这一结果使。这一结果使Temin Temin Tem

10、in Temin 的的的的“前病前病前病前病毒毒毒毒”假想得到了证实。假想得到了证实。假想得到了证实。假想得到了证实。l l1975197519751975年年年年TeminTeminTeminTemin、BaltimoveBaltimoveBaltimoveBaltimove和和DulbaccoDulbaccoDulbaccoDulbacco因此获诺贝尔生理因此获诺贝尔生理因此获诺贝尔生理因此获诺贝尔生理和医学奖。和医学奖。和医学奖。和医学奖。第十二页，讲稿共一百五十五页哦The Nobel Prize in Physiology or Medicine 1975 The interacti

11、on between tumor viruses and the genetic material of the cell第十三页，讲稿共一百五十五页哦David B BaltimoreUSAMassachusetts Institute ofTechnology(MIT)Cambridge,MA,USAB:1938第十四页，讲稿共一百五十五页哦Renato DulbeccoUSAImperial Cancer ResearchFund LaboratoryLondon,United KingdomB:1914(in Catanzaro,Italy)第十五页，讲稿共一百五十五页哦Howard

12、Martin TeminUSAUniversity of WisconsinMadison,WI,USAB:1934D:1994第十六页，讲稿共一百五十五页哦BishopBishop和和VarmusVarmus等人于等人于19801980年提出了年提出了癌基因假说癌基因假说，认为认为RousRous鸡肉瘤病毒的致癌能力与病毒基因组的鸡肉瘤病毒的致癌能力与病毒基因组的单个基因有关，即单个基因有关，即srcsrc基因。基因。srcsrc基因本是正常细胞基因组的一部分基因本是正常细胞基因组的一部分(原癌基因）原癌基因），被病毒，被病毒“劫持劫持”后，病毒则具有致癌能力。后，病毒则具有致癌能力。原癌基

13、因在正常细胞中的地位：调控细胞的分裂原癌基因在正常细胞中的地位：调控细胞的分裂和生长。和生长。肿瘤细胞中癌基因的变化：过分活跃或突变，使肿瘤细胞中癌基因的变化：过分活跃或突变，使其编码产物改变。其编码产物改变。BishopBishop和和VarmuVarmus s获获19891989年诺贝尔生理学和医学奖年诺贝尔生理学和医学奖第十七页，讲稿共一百五十五页哦The Nobel Prize in Physiology or Medicine 1989 The cellular origin of retroviral oncogenes第十八页，讲稿共一百五十五页哦J.Michael Bishop

14、USAUniversity of CaliforniaSchool MedicineSan Francisco,CA,USAB:1936第十九页，讲稿共一百五十五页哦Harold E.VarmusUSAUniversity of CaliforniaSchool of MedicineSan Francisco,CA,USAB:1939第二十页，讲稿共一百五十五页哦Press Release:The 1989 Nobel Prize in Physiology or MedicineNOBELFRSAMLINGEN KAROLINSKA INSTITUTETTHE NOBEL ASSEMBLY

15、 AT THE KAROLINSKA INSTITUTE9October1989The Nobel Assembly at Karlinska InstitutehastodaydecidedtoawardtheNobelPrizeinPhysiologyorMedicinefor1989jointlytoJ.Michael Bishop and Harold E.Varmusfortheirdiscoveryofthecellularoriginofretroviraloncogenes.Press Release第二十一页，讲稿共一百五十五页哦SummaryThediscoveryawar

16、dedwiththisyearsNobelPrizeinPhysiologyorMedicineconcernstheidentificationofalargefamilyofgeneswhichcontrolthenormalgrowthanddivisionofcells.Distur-bancesinoneorsomeoftheseso-calledoncogenes(Gknco(s)Bulk,mass)canleadtotransformationofanormalcellintoatumorcellandresultincancer.Michael BishopandHarold

17、Varmususedanoncogenicretrovirustoidentifythegrowth-controllingoncogenesinnormalcells.In1976theypublishedtheremarkableconclusionthattheoncogeneinthevirusdidnotrepresentatrueviralgenebutinsteadwasanormalcellulargene,whichthevirushadacquiredduringreplicationinthehostcellandthereaftercarriedalong.第二十二页，

18、讲稿共一百五十五页哦BishopsandVarmusdiscoveryofthecellularoriginofretroviraloncogeneshashadanextensiveinfluenceonthedevelopmentofourknowledgeaboutmechanismsfortumordevelopment.Untilnowmorethan40differentoncogeneshavebeendemonstrated.Thediscoveryhasalsowidenedourinsightintothecomplicatedsignalsystemswhichgover

19、nthenormalgrowthofcells.Cellular Oncogenes Discovered by the Use of RetrovirusThetermoncogenewasintroducedinthemiddleofthe1960stodenotespecialpartsofthegeneticmaterialofcertainviruses.Itwasbelievedthatthispartofthegeneticmaterialcoulddirectthetransformationofanormalcellintoatumorcellundertheinfluenc

20、eofotherpartsoftheviralgeneticmaterial,alternativelyviachemicalorphysicaleffects.Thefavouritetheoryofthetimewasthatvirus-mediatedcell-to-celltransmittanceofoncogeneswastheoriginofallformsofcancer.Thisviewwaslaterproventobeincorrect.第二十三页，讲稿共一百五十五页哦Theoriginaldiscoveryofanoncogenicviruswasmadein1916b

21、yPeyton RousworkingattheRockefellerInstituteinNewYork.FiftyyearslaterRousreceivedtheNobelPrizeinPhysiologyorMedicine.Rousvirus,astheinfectiousagentlaterwasnamed,isamemberofalargevirusfamilynamedretroviruses.ThegeneticmaterialofthesevirusesisRNA(ribonucleicacid).ThisRNAcanbetranscribedintoDNA(deoxyri

22、bonucleicacid)byauniqueenzymeinthevirus,reversetranscriptase.The1975NobelPrizeinPhysiologyorMedicinewasawardedtoDavidBaltimore,RenatoDulbeccoandHawardTeminpartlyforthediscoveryofthisenzyme.ReversetranscriptionofthegeneticmaterialofthevirusintoDNAhastheimportantconsequencethatitcanbecomeintegratedint

23、othechromosomalDNAinthecells.ItwasthroughinvestigationsofRousvirusthatthisyearslaureatesMichael BishopandHarold Varmusin1975coulddemonstratethetrueoriginofoncogenes.TheyusedonevariantofRousviruswhichcontainedanoncogenicgene(Figure1)andanothervariantwhichlackedthisgene.第二十四页，讲稿共一百五十五页哦Byuseofthesevir

24、usestheymanagedtoconstructanucleicacidprobewhichselectivelyidentifiedtheoncogene.ThisprobewasusedtosearchforthecorrespondinggeneticmaterialinDNAfromdifferentcells.Itwasthenfoundthatoncogene-likematerialcouldbedetectedindifferentspeciesthroughouttheanimalkingdom,infacteveninsimpleorganismscomprisingo

25、nlyafewcells.Furthermore,itwasshownthatthegenehadafixedpositioninthechromosomesofacertainspecies,andthatthegene,whenitconstitutedpartofthecellulargeneticmaterial,wasdividedintofragments(amosaicgene)(Figure1).Figure 1.Thedifferencebetweenanoncogeneinavirusandinacell.Inretrovirusescausingtumorsthereis

26、aseparatesegmentoftransformingnucleicacidwhichhasbeenderivedfromacell.Thecellulargeneissplit(amosaicgene)whereastheoncogeneinthevirusiscontinuous.第二十五页，讲稿共一百五十五页哦Thesefindingsledtotheremarkableconclusionthattheoncogeneinthevirusdidnotrepresentatrueviralgenebutacellulargenewhichthevirushadpickedupfar

27、backduringitsreplicationincellsandcarriedalong.Thiscellulargenewasfoundtohaveacentralfunctioninthecells.Itcontrolledtheirgrowthanddivision.Throughthesestudiesoftheabnormal,i.e.thediseasedstate,itwaspossibletoelucidatecriticalnormalcellularfunctions-anotuncommonsituationinbiomedicalresearch.Theorigin

28、aldiscoveryofacellularoncogeneledtoanintensivesearchforfurthersimilargenes.Theexplosivedevelopmentofthisfieldofresearchhasledtotheidentificationofmorethan40differentoncogeneswhichdirectdifferenteventsinthecomplexsignalsystemsthatregulatethegrowthanddivisionofcells.Changesinanyoneormoreoftheseoncogen

29、esmayleadtocancer.第二十六页，讲稿共一百五十五页哦Balanced Cellular Interactions-A Biological WonderSymmetricalandasymmetrical,multicellularstructuresdevelopfromthefertilizedovumbyaprocessofdifferentiationaboutwhichonlylimitedknowledgeisavailable.Inthefullydevelopedindividualcarefullybalancedconditionsprevail.Damag

30、eofanorganelicitssophisticatedrepairprocesseswhichleadtorestitutionoftheoriginalconditionoftheorgan.However,ifasinglecellescapesthenetworkofgrowthcontroltheresultmaybeanabnormallocalproliferationofcellsorintheworstcaseacancerimplyingthedisseminationofcellsrunningamok.Thedevelopmentofacancerisacompli

31、catedprocessinvolvingseveralconsecutivechangesofthegeneticmaterial.Studiesofcellulargenes(proto-oncogenes)correspondingtotheviraloncogenes,hasstartedtoshedlightontheintricatesystemswhichcontrolnormalcellulargrowthanddivision.第二十七页，讲稿共一百五十五页哦Cellular Oncogene Products Constitute Links in Signal Chain

32、s which Regulate Growth and Division of CellsTheregulationofgrowthanddivisionofcellshasturnedouttobemuchmorecomplicatedthanoriginallybelieved.Cellularoncogeneproductswithdifferentpropertiesactindifferentpositionsofelaboratesignalsystems(Figure2).Inordertotransmitsignalsfromonecelltotheotherorfromone

33、celltoitselftherearegrowthfactors.Thesefactorsappearinthefluidssurroundingcells.Thereareexamplesofoncogeneproducts,viz.proteinsproducedinthecytoplasm,whichcanactasgrowthfactors.Thus,itwasfoundthattheproductofthesis1)genewascloselyrelatedtoapreviouslyidentifiedgrowthfactorPDGF(PlateletDerivedGrowthFa

34、ctor).第二十八页，讲稿共一百五十五页哦Figure 2.Oncogene products are links in signal chains that stretch from the cell surface to the genetic material in the cell nucleus.This chain is composed of(1)growth factors,(2)growth factor receptors,(3)signal transducing proteins in cell membranes,(4)phosphokinases in the c

35、ytoplasm and(5)proteins transported from the cytoplasm into the nucleus where they bind to DNA.The localization of different oncogene products(Sis,ErbB,Ras,Src,Myc)is schematically indicated.第二十九页，讲稿共一百五十五页哦In order for a growth factor to be able to interact with a cell there has to be membrane stru

36、ctures,receptors,to which they can bind.There are several oncogene products which represent receptors in the cytoplasmic membrane of the cells,e.g.ErbA,Fms,Kit.These receptors have a unique enzymatic activity.They are so-called kinases with a capacity to phosphorylate(=add a phosphate group)the amin

37、o acid tyrosine.There are two more groups of oncogene products with phosphokinase activity;firstly tyrosine/phospho-kinase which lack receptor function and is located at the inside of the cytoplasmic membrane,and secondly serine/threonine phosphokinase which is found in the cytoplasm.Thus,oncogene p

38、roducts function as links in signal chains stretching from the surface of the cell to the genetic material in the nucleus.In the cytoplasm there is one more group of oncogene products.These are called Ras and are related to important cellular signal factors called G-proteins.Finally,there is a large

39、 number of oncogene products which are located in the nucleus of the cell,i.e.Myc,Myb,Fos,ErbA and others.These products direct the transcription of DNA into RNA and therefore play a critical role in the selection of proteins to be synthesized by the cell.第三十页，讲稿共一百五十五页哦Cancer-A Complex,Biological S

40、equence of EventsChanges in the genetic material constitute the basis for the development of all cancer.Generally there are several consecutive such changes which influence different steps in the signal chains described above.Therefore,one should priori not expect to find one single clue to the mech

41、anism of origin of cancer.However,application of the expanding knowledge in the oncogene field allows us to start comprehending the disharmonic orchestration behind abnormal cellular growth.It is conceptually incorrect to speak about cancer genes.However,historical circumstances explain why the onco

42、gene terminology was introduced before a designation of the corresponding normal cellular genes was proposed.From the point of view of cancer the important matter is to compare oncogenes in normal cells and in tumor cells.第三十一页，讲稿共一百五十五页哦Oncogenes as a Cause of CancerThe majority of oncogenes have b

43、een discovered in experimental studies using retroviruses.However,in a few cases oncogenes were identified bythe use of an alternative technique,i.e.genetic material was isolated from tumor cells of non-viral origin and transferred(transfected)to other cells prapagated in culture.The cells receiving

44、 the DNA changed growth pattern,and further characterization of the transfected genetic material revealed the presence of oncogenes.Two principally different forms of activation of oncogenes can be distinguished.Firstly,the normal cellular oncogene is hyperactive,and secondly the oncogene product is

45、 altered so that it can no longer be regulated in a normal way.There are several examples of these types of activation of oncogenes.The discovery of oncogenes was as mentioned originally made by the use of retroviruses.This infers that genetic control elements in the virus itself can be responsible

46、for the abnormal expression of the oncogene.However,in many cases it was found that alterations of the transferred oncogene contributed to its accentuated expression.第三十二页，讲稿共一百五十五页哦There are retroviruses which lack oncogenes but still can induce cancer.This is due to the fact that the virus has ins

47、erted its genetic material(in the form of DNA)very close to a normally occurring oncogene in the genetic material of the cell.This may result in an increased turn-over of the oncogene which may lead to abnormal cellular growth.The corresponding phenomenon can also occur in the absence of retroviruse

48、s.In this case there is a reorgani-zation of the genetic material in the cell.Such a reorganization may occur within a single chromosome or by exchange of material between chromosomes.Repeated copying of a normal oncogene can lead to its amplification in the chromosome and consequently to increased

49、amounts of the oncogene product.In certain brain tumors,glioblastomas,an amplified erbB-gene has been found,and a correspondingly increased neu-gene activity was shown in some forms of breast cancer.The same effect can be seen when there is a reciprocal exchange of segments between chromosomes(trans

50、location).Thus the normal myc-gene on chromosome 8 has been translocated to chromosome 14 in many patients with Burkitts lymphomas(Figure 3).The insertion of the myc-gene containing chromosome segment is such that it becomes located close to hyperactive genes directing the synthesis of antibody prot