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Tumor cell-specific AIM2 regulates growth and invasion of cutaneous squamous cell carcinoma

Nissinen L; Quint KD; Kivisaari A; Riihilä P; Peltonen S; Kähäri VM; Farshchian M; Piipponen M; Grénman R; Bavinck JNB; Kallajoki M; Siljamäki E; Peltonen J

dc.contributor.authorNissinen L
dc.contributor.authorQuint KD
dc.contributor.authorKivisaari A
dc.contributor.authorRiihilä P
dc.contributor.authorPeltonen S
dc.contributor.authorKähäri VM
dc.contributor.authorFarshchian M
dc.contributor.authorPiipponen M
dc.contributor.authorGrénman R
dc.contributor.authorBavinck JNB
dc.contributor.authorKallajoki M
dc.contributor.authorSiljamäki E
dc.contributor.authorPeltonen J
dc.date.accessioned2022-10-28T14:14:08Z
dc.date.available2022-10-28T14:14:08Z
dc.identifier.urihttps://www.utupub.fi/handle/10024/170173
dc.description.abstract<p>Cutaneous squamous cell carcinoma (cSCC) is the most common metastatic skin cancer. Inflammation is a typical feature in cSCC progression. Analysis of the expression of inflammasome components in cSCC cell lines and normal human epidermal keratinocytes revealed upregulation of the expression of AIM2 mRNA and protein in cSCC cells. Elevated levels of AIM2 mRNA were noted in cSCCs in vivo compared with normal skin. Strong and moderate tumor cell specific expression of AIM2 was detected with immunohistochemistry (IHC) in sporadic human cSCCs in vivo, whereas expression of AIM2 was moderate in cSCC in situ (cSCCIS) and low or absent in actinic keratosis (AK) and normal skin. IHC of cSCCs, cSCCIS and AKs from organ transplant recipients also revealed strong and moderate tumor cell specific expression of AIM2 in cSCCs. Knockdown of AIM2 resulted in reduction in viability of cSCC cells and onset of apoptosis. RNA-seq and pathway analysis after knockdown of AIM2 in cSCC cells revealed downregulation of the biofunction category Cell cycle and upregulation of the biofunction category Cell Death and Survival. Knockdown of AIM2 also resulted in reduction in invasion of cSCC cells and downregulation in production of invasion proteinases MMP1 and MMP13. Knockdown of AIM2 resulted in suppression of growth and vascularization of cSCC xenografts in vivo. These results provide evidence for the role of AIM2 in the progression of cSCC and identify AIM2 inflammasome function as a potential therapeutic target in these invasive and metastatic tumors.<br /></p>
dc.language.isoen
dc.publisherImpact Journals LLC
dc.titleTumor cell-specific AIM2 regulates growth and invasion of cutaneous squamous cell carcinoma
dc.identifier.urnURN:NBN:fi-fe2021042717144
dc.relation.volume8
dc.contributor.organizationfi=tyks, vsshp|en=tyks, vsshp|
dc.contributor.organizationfi=iho- ja sukupuolitautioppi|en=Dermatology and Venereology|
dc.contributor.organizationfi=lääket. tdk yhteiset|en=Lääket. tdk yhteiset|
dc.contributor.organizationfi=biolääketieteen laitos, yhteiset|en=Institute of Biomedicine|
dc.contributor.organizationfi=lastentautioppi|en=Paediatrics and Adolescent Medicine|
dc.contributor.organization-code2607000
dc.contributor.organization-code2607100
dc.contributor.organization-code2607313
dc.contributor.organization-code2607305
dc.converis.publication-id26504305
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/26504305
dc.format.pagerange45836
dc.format.pagerange45825
dc.identifier.jour-issn1949-2553
dc.okm.affiliatedauthorKallajoki, Markku
dc.okm.affiliatedauthorFarshchian, Mehdi
dc.okm.affiliatedauthorPiipponen, Minna
dc.okm.affiliatedauthorGrenman, Reidar
dc.okm.affiliatedauthorNissinen, Liisa
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.affiliatedauthorKähäri, Veli-Matti
dc.okm.affiliatedauthorRiihilä, Pilvi
dc.okm.affiliatedauthorPeltonen, Sirkku
dc.okm.affiliatedauthorPeltonen, Juha
dc.okm.affiliatedauthorKivisaari, Atte
dc.okm.affiliatedauthorSiljamäki, Elina
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.discipline319 Forensic science and other medical sciencesen_GB
dc.okm.discipline319 Oikeuslääketiede ja muut lääketieteetfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeJournal article
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.18632/oncotarget.17573
dc.relation.ispartofjournalOncotarget
dc.relation.issue28
dc.year.issued2017


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