Juho Suojanen

Dr. Juho Suojanen

orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 December 2016 in Journal of Cranio-Maxillofacial Surgery
Verified
Journal Article
Closed access
Juho SuojanenJuho Suojanen
Juho Suojanen
JLJunnu Leikola
Junnu Leikola
PSPatricia Stoor
Patricia Stoor

1 July 2019 in Journal of Cranio-Maxillofacial Surgery
Verified
Journal Article
Closed access
SJS. Järvinen
S. Järvinen
Juho SuojanenJuho Suojanen
Juho Suojanen
EKE. Kormi
E. Kormi
TWT. Wilkman
T. Wilkman
AKA. Kiukkonen
A. Kiukkonen
PSP. Stoor
P. Stoor

1 June 2017 in Journal of Cranio-Maxillofacial Surgery
Verified
Journal Article
Closed access
Juho SuojanenJuho Suojanen
Juho Suojanen
JLJunnu Leikola
Junnu Leikola
PSPatricia Stoor
Patricia Stoor

5 December 2012 in PLOS ONE
Verified
Journal Article
Open access
PDF file
MAMari Aikio
Mari Aikio
IAIlkka Alahuhta
Ilkka Alahuhta
SNSini Nurmenniemi
Sini Nurmenniemi
Juho SuojanenJuho Suojanen
Juho Suojanen
RPRiitta Palovuori
Riitta Palovuori
PNPia Nyberg
Pia Nyberg
The turnover of extracellular matrix liberates various cryptic molecules with novel biological activity. Among these are the collagen-derived anti-angiogenic fragments, some of which are suggested to affect carcinoma cells also directly. Arresten is an endogenous angiogenesis inhibitor that is derived from the non-collagenous domain of the basement membrane collagen IV α1 chain. As the mere prevention of tumor angiogenesis leads to hypoxia that can result in selection of more aggressive cell types and reduces the efficacy of chemotherapy, we aimed here to elucidate how arresten influences the aggressive human carcinoma cells. Arresten efficiently inhibited migration and invasion of HSC-3 tongue carcinoma cells in culture and in an organotypic model. Subcutaneous Arr-HSC xenografts grew markedly more slowly in nude mice and showed reduced tumor cell proliferation, vessel density and local invasiveness. In the organotypic assay, HSC-3 cells overproducing arresten (Arr-HSC) showed induction of cell death. In monolayer culture the Arr-HSC cells grew in aggregated cobblestone-like clusters and, relative to the control cells, showed increased expression and localization of epithelial marker E-cadherin in cell-cell contacts. Application of electric cell-substrate impedance sensing (ECIS) further supported our observations on altered morphology and motility of the Arr-HSC cells. Administration of a function-blocking α1 integrin antibody abolished the impedance difference between the Arr-HSC and control cells suggesting that the effect of arresten on promotion of HSC-3 cell-cell contacts and cell spreading is at least partly mediated by α1β1 integrin. Collectively, our data suggest novel roles for arresten in the regulation of oral squamous carcinoma cell proliferation, survival, motility and invasion through the modulation of cell differentiation state and integrin signaling.

15 December 2009 in Cancer Biology & Therapy
Verified
Journal Article
Closed access
Juho SuojanenJuho Suojanen
Juho Suojanen
TSTuula Salo
Tuula Salo
EKErkki Koivunen
Erkki Koivunen
TSTimo Sorsa
Timo Sorsa
EPEmma Pirilä
Emma Pirilä
Matrix metalloproteinases (MMPs), and especially membrane type-1 matrix metalloproteinase (MT1-MMP, MMP-14), play a role in cancer progression and can have a prognostic value. Various synthetic bro...

1 July 2019 in Journal of Cranio-Maxillofacial Surgery
Verified
Journal Article
Closed access
KKKaroliina V.M. Kotaniemi
Karoliina V.M. Kotaniemi
AHArja Heliövaara
Arja Heliövaara
MKMiika Kotaniemi
Miika Kotaniemi
PSPatricia Stoor
Patricia Stoor
JLJunnu Leikola
Junnu Leikola
Juho SuojanenJuho Suojanen
Juho Suojanen