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Research Hypothesis - Rough Draft
Research Hypothesis - Rough Draft
SaharMahate
InternMentorIG/T
20172018
Title:T umorDormancyinOsteosarcoma
ResearchQuestion:
Howwillthediscoveryoftumordormancyaltercurrentcancertreatments?
Hypothesis:
Ifdormanttumorcellsarefoundinalivingorganism,drugsworkingtopreventangiogenesis
couldbeusedtopreventproliferationofthetumorcells.
Background/HistoryoftheIssue:
TumordormancyoccurswhentumorcellsenteranextendedG0phase(Naumov,Akslen&
Folkman,2006).Tumorsdependonangiogenesistogrow,andarethusareharmlesswheninthe
nonangiogenicdormantstate.Anearlydemonstrationoftumordormancywasseeninarabbit
eye,asthetumorintherabbiteyeremainedstagnantuntilthecellsweremovedclosertoiris
vessels,whichallowedthetumorcellstoformnewbloodvesselssothatitcouldspread.
Neovascularizationinirisvesselsdemonstratedthetumorsreleaseofangiogenicfactorswhich
causedthetumortogrowexponentially.
Rationale:
Thistopicishugelyimportantbecauseunderstandingtumordormancycanallowmoreeffective
treatmentstobeusedtopreventorstopcancermetastasis.
BasisofHypothesis:
Myhypothesisisbasedonresearchabouttumordormancyandtheprocessofangiogenesis.If
dormanttumorcellscanbefoundintheanimalmodels,treatmentstopreventthecellsfrom
undergoingangiogenesiscanberesearchedinordertofacilitatetumordormancyandprevent
cancer.
OperationalDefinitions:
Angiogenesistheformationofnewbloodvessels
DescriptorsUsedforLiteratureSearch:
Tumordormancy
Dormanttumorcells
G0phasetumorcells
Nonangiogenictumorcells
Angiogenesisincancercells
References
Naumov,G.N.,Akslen,L.A.,&Folkman,J.(2006,August15).Roleofangiogenesisinhuman
tumordormancy:Animalmodelsoftheangiogenicswitch.RetrievedOctober7,2017,
fromhttps://www.ncbi.nlm.nih.gov/pubmed/16931911