TY - JOUR
T1 - Immunohistochemical analysis of transcription factors and markers of epithelial-mesenchymal transition (EMT) in human tumors
AU - Ghulam, Jasamin
AU - Stuerken, Christine
AU - Wicklein, Daniel
AU - Pries, Ralph
AU - Wollenberg, Barbara
AU - Schumacher, Udo
N1 - Publisher Copyright:
© 2019 International Institute of Anticancer Research. All rights reserved.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2019/10
Y1 - 2019/10
N2 - Background/Aim: Epithelial-mesenchymal transition (EMT) is a key multi-step process which enables cancer cells to detach from the epithelial primary tumor mass and allows them to metastasize to distant organs. We immunohistochemically analyzed the expression of the transcription factors (TWIST-1, SLUG, ZEB1, ZEB2) and components of the extracellular matrix (laminin-5, fibronectin) which influence the EMT. Materials and Methods: Primary human breast (MDA-MB-231), colon (HT29, HCT116), ovarian (SKOV3, OVCAR3) and head and neck squamous cell carcinoma cell lines (UTSCC2, UTSCC24A) grown as xenografts were immunohistochemically analyzed in vitro and in vivo. Results: A high SLUG expression was observed in every cancer entity both in vitro and in vivo. ZEB1 and ZEB2 showed a high in vivo expression especially in SKOV3 and in in vitro grown MDA-MB-231 cells. Conclusion: SLUG expression showed the highest expression in all cancer entities investigated. Hence, it presumably represents the master regulator of EMT in these metastatic tumor entities.
AB - Background/Aim: Epithelial-mesenchymal transition (EMT) is a key multi-step process which enables cancer cells to detach from the epithelial primary tumor mass and allows them to metastasize to distant organs. We immunohistochemically analyzed the expression of the transcription factors (TWIST-1, SLUG, ZEB1, ZEB2) and components of the extracellular matrix (laminin-5, fibronectin) which influence the EMT. Materials and Methods: Primary human breast (MDA-MB-231), colon (HT29, HCT116), ovarian (SKOV3, OVCAR3) and head and neck squamous cell carcinoma cell lines (UTSCC2, UTSCC24A) grown as xenografts were immunohistochemically analyzed in vitro and in vivo. Results: A high SLUG expression was observed in every cancer entity both in vitro and in vivo. ZEB1 and ZEB2 showed a high in vivo expression especially in SKOV3 and in in vitro grown MDA-MB-231 cells. Conclusion: SLUG expression showed the highest expression in all cancer entities investigated. Hence, it presumably represents the master regulator of EMT in these metastatic tumor entities.
UR - http://www.scopus.com/inward/record.url?scp=85072763035&partnerID=8YFLogxK
U2 - 10.21873/anticanres.13737
DO - 10.21873/anticanres.13737
M3 - Journal articles
C2 - 31570438
AN - SCOPUS:85072763035
SN - 0250-7005
VL - 39
SP - 5437
EP - 5448
JO - Anticancer Research
JF - Anticancer Research
IS - 10
ER -