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dc.contributor.advisorJokela, Tiina
dc.contributor.advisorIhalainen, Janne
dc.contributor.authorKärkkäinen, Minta
dc.date.accessioned2023-06-30T04:57:05Z
dc.date.available2023-06-30T04:57:05Z
dc.date.issued2023
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/88138
dc.description.abstractLynch syndrome is an inherited cancer-predisposing syndrome where occur mutations in mismatch repair genes. Colorectal cancer is a common form of cancer within Lynch syndrome carriers. The inherited gene mutation predisposes to the development of colorectal cancer, but diet, especially red meat, fiber, and calcium intake, is known to significantly impact cancer development. Currently, there is limited information on what kind of molecular mechanisms mediate the effect of nutrition on colorectal cancer risk within Lynch syndrome carriers. Recent studies have indicated the importance of circulating non-coding RNAs, like microRNAs, in cancer development. Circulating microRNAs are small approximately 20 nucleotide long molecules in the bloodstream that regulate several biological processes. Circulating microRNA expression patterns change in connection with cancer. This thesis aimed to study whether red meat, fiber, and calcium daily intake are associated with circulating microRNA expression levels of Lynch syndrome carriers. The associations between nutrient intake and circulating microRNA expression levels were studied using the Spearman rank correlation coefficient and multiple linear regression analysis. The statistical tests revealed significant associations between these variables where hsa-miR-3613-5p was specifically associated with red meat intake and hsa-miR-144-5p with fiber intake. The possible function of hsa-miR-3613-5p and hsa-miR-144-5p in colorectal cancer was studied by transfecting appropriate microRNA mimics in patient-derived colorectal cancer organoids and by performing cell viability and apoptosis assays to the transfected cells. Hsa-miR-144-5p reduced the viability of colorectal cancer cells and in addition induced apoptosis in these cells. Hsa-miR-3613-5p had no clear effect on the viability of the studied cancer cells. The study suggests nutrition has an impact on circulating microRNA expression levels. In addition, these microRNAs associated with diet may enhance or suppress colorectal cancer cell growth.en
dc.format.extent57
dc.language.isoen
dc.rightsIn Copyright
dc.subject.otherhereditary colorectal cancer
dc.titleCirculating microRNAs are a potential molecular link between nutrition and colorectal cancer risk in Lynch Syndrome
dc.identifier.urnURN:NBN:fi:jyu-202306304284
dc.type.ontasotMaster’s thesisen
dc.type.ontasotPro gradu -tutkielmafi
dc.contributor.tiedekuntaMatemaattis-luonnontieteellinen tiedekuntafi
dc.contributor.tiedekuntaFaculty of Sciencesen
dc.contributor.laitosBio- ja ympäristötieteiden laitosfi
dc.contributor.laitosDepartment of Biological and Environmental Scienceen
dc.contributor.yliopistoJyväskylän yliopistofi
dc.contributor.yliopistoUniversity of Jyväskyläen
dc.contributor.oppiaineSolu- ja molekyylibiologiafi
dc.contributor.oppiaineCell and molecular biologyen
dc.rights.copyright© The Author(s)
dc.rights.accesslevelrestrictedAccess
dc.contributor.oppiainekoodi4013
dc.subject.ysoravinto
dc.subject.ysoepigenetiikka
dc.subject.ysoepidemiologia
dc.subject.ysomikro-RNA
dc.subject.ysopaksusuolisyöpä
dc.subject.ysoLynchin oireyhtymä
dc.subject.ysoravitsemus
dc.subject.ysoperäsuolisyöpä
dc.subject.ysonutrition
dc.subject.ysoepigenetics
dc.subject.ysoepidemiology
dc.subject.ysomicroRNA
dc.subject.ysocancer of the large intestine
dc.subject.ysoLynch syndrome
dc.subject.ysodietetics
dc.subject.ysorectal cancer
dc.rights.urlhttps://rightsstatements.org/page/InC/1.0/
dc.rights.accessrightsThe author has not given permission to make the work publicly available electronically. Therefore the material can be read only at the archival workstation at Jyväskylä University Library (https://kirjasto.jyu.fi/collections/archival-workstation).en
dc.rights.accessrightsTekijä ei ole antanut lupaa avoimeen julkaisuun, joten aineisto on luettavissa vain Jyväskylän yliopiston kirjaston arkistotyösemalta. Ks. https://kirjasto.jyu.fi/kokoelmat/arkistotyoasema..fi


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