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Comparative proteogenomic analysis of right-sided colon cancer, left-sided colon cancer and rectal cancer reveals distinct mutational profiles

dc.contributor.authorImperial, Robin
dc.contributor.authorAhmed, Zaheer
dc.contributor.authorToor, Omer M.
dc.contributor.authorErdogan, Cihat
dc.contributor.authorKhaliq, Ateeq
dc.contributor.authorCase, Paul
dc.contributor.authorCase, James
dc.contributor.authorKennedy, Kevin
dc.contributor.authorCummings, Lee S.
dc.contributor.authorMelton, Niklas
dc.contributor.authorRaza, Shahzad
dc.contributor.authorDiri, Banu
dc.contributor.authorMohammad, Ramzi
dc.contributor.authorEl-Rayes, Bassel
dc.contributor.authorPluard, Timothy
dc.contributor.authorHussain, Arif
dc.contributor.authorSubramanian, Janakiraman
dc.contributor.authorMasood, Ashiq
dc.date.accessioned2026-06-27T14:16:08Z
dc.date.issued2018
dc.description.abstractRight-sided colon cancer (RCC) has worse prognosis compared to left-sided colon cancer (LCC) and rectal cancer. The reason for this difference in outcomes is not well understood. We performed comparative somatic and proteomic analyses of RCC, LCC and rectal cancers to understand the unique molecular features of each tumor sub-types. Utilizing a novel in silico clonal evolution algorithm, we identified common tumor-initiating events involving APC, KRAS and TP53 genes in RCC, LCC and rectal cancers. However, the individual role-played by each event, their order in tumor development and selection of downstream somatic alterations were distinct in all three anatomical locations. Some similarities were noted between LCC and rectal cancer. Hotspot mutation analysis identified a nonsense mutation, APC R1450* specific to RCC. In addition, we discovered new significantly mutated genes at each tumor location, Further in silico proteomic analysis, developed by our group, found distinct central or hub proteins with unique interactomes among each location. Our study revealed significant differences between RCC, LCC and rectal cancers not only at somatic but also at proteomic level that may have therapeutic relevance in these highly complex and heterogeneous tumors.en
dc.description.sponsorshipMerit Review Award, Medical Research Service, Department of Veterans Affairs [I01 BX000545]
dc.description.urihttps://doi.org/10.1186/s12943-018-0923-9
dc.identifier.doi10.1186/s12943-018-0923-9
dc.identifier.eissn1476-4598
dc.identifier.pubmed30577807
dc.identifier.urihttps://hdl.handle.net/20.500.14981/58656
dc.identifier.volume17
dc.identifier.wos000454253100001
dc.language.isoeng
dc.publisherBMC
dc.relation.ispartofMOLECULAR CANCER
dc.rightsopenAccess
dc.subjectRight-sided colon cancer
dc.subjectLeft-sided colon cancer
dc.subjectRectal cancers
dc.subjectClonal evolution
dc.subjectProteomics
dc.subjectHotspot mutations
dc.subjectBiochemistry & Molecular Biology
dc.subjectOncology
dc.titleComparative proteogenomic analysis of right-sided colon cancer, left-sided colon cancer and rectal cancer reveals distinct mutational profiles
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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