Orest W. Blaschuk
Research Subjects
Orest W. Blaschuk has a total of 17 co-authors. Here are the top co-authors by number of shared publications:
Alaknanda Emery
Robinson Research Institute, Adelaide Medical School, The University of Adelaide
1 shared publicationAndrew Cw Zannettino
Myeloma Research Laboratory, Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia. South Australian Health and Medical Research Institute, Adelaide, Australia. Central Adelaide Local Health Network
1 shared publicationAndrew D Abell
Department of Chemistry, The University of Adelaide
1 shared publication- Concepcion Maria Aguilera
Centro de Investigación Biomédica en Red de Fisiopatología de la Obesidad y la Nutrición (CIBEROBN), Instituto de Salud Carlos III, Madrid, Spain; Department of Biochemistry and Molecular Biology II, Institute of Nutrition and Food Technology (INYTA) and Center of Biomedical Research (CIBM), University of Granada, Granada, 18071, Spain; Instituto de Investigación Biosanitaria ibs.GRANADA, Granada, Spain
1 shared publication - Cressida A. Lyon
Department of Life Sciences, University of Bath, Bath, United Kingdom
1 shared publication - Darryl Lyndon Russell
University of Adelaide
1 shared publication
Latest Publications
- Open Access
- 29 July 2025
- Published by eLife Sciences Publications, Ltd in eLife
- Vol. 13
N-cadherin mechanosensing in ovarian follicles controls oocyte maturation and ovulation
The cell adhesion molecule N-cadherin (CDH2) is a membrane component of adherens junctions which regulates tissue morphogenesis and architecture. In the follicles of mammalian ovaries, N-cadherin adherens junctions are present between granulosa cells, cumulus cells, and at the interface of cumulus cell transzonal projections and the oocyte. We demonstrate a mechanosensory role of N-cadherin integrating tissue structure and hormonal regulation of follicular morphogenic events including expansion of the cumulus–oocyte complex (COC) matrix, oocyte maturation, and ovulation. Two small molecule N-cadherin antagonists inhibited COC maturation in vitro. Transcriptome profiling revealed that targets of β-catenin and YAP1 pathways were dysregulated by N-cadherin antagonists. In vivo, N-cadherin antagonist significantly reduced ovulation in mice compared to controls (11 vs 26 oocytes/ovary; p = 5.8 × 10−6). Ovarian follicles exhibited structural dysgenesis with granulosa and cumulus cell layers becoming disorganised and the connection between cumulus cells and the oocyte disrupted and the transcriptome again indicated altered mechanical sensing causing dysregulation of the Hippo/YAP and β-catenin pathways and extracellular matrix reorganisation. Granulosa-specific N-cadherin depletion in Cdh2Fl/FL;Amhr2Cre/+ also showed significantly altered mechanosensitive gene expression and reduced ovulation. Our findings demonstrate a critical role for N-cadherin in ovarian follicular development and ovulation, and the potential to inhibit ovulation through targeting this signalling mechanism.
- 29 July 2025
- Published by eLife Sciences Publications, Ltd in eLife
- Vol. 13
Open AccessN-cadherin mechanosensing in ovarian follicles controls oocyte maturation and ovulation
The cell adhesion molecule N-cadherin (CDH2) is a membrane component of adherens junctions which regulates tissue morphogenesis and architecture. In the follicles of mammalian ovaries, N-cadherin adherens junctions are present between granulosa cells, cumulus cells, and at the interface of cumulus cell transzonal projections and the oocyte. We demonstrate a mechanosensory role of N-cadherin integrating tissue structure and hormonal regulation of follicular morphogenic events including expansion of the cumulus–oocyte complex (COC) matrix, oocyte maturation, and ovulation. Two small molecule N-cadherin antagonists inhibited COC maturation in vitro. Transcriptome profiling revealed that targets of β-catenin and YAP1 pathways were dysregulated by N-cadherin antagonists. In vivo, N-cadherin antagonist significantly reduced ovulation in mice compared to controls (11 vs 26 oocytes/ovary; p = 5.8 × 10−6). Ovarian follicles exhibited structural dysgenesis with granulosa and cumulus cell layers becoming disorganised and the connection between cumulus cells and the oocyte disrupted and the transcriptome again indicated altered mechanical sensing causing dysregulation of the Hippo/YAP and β-catenin pathways and extracellular matrix reorganisation. Granulosa-specific N-cadherin depletion in Cdh2Fl/FL;Amhr2Cre/+ also showed significantly altered mechanosensitive gene expression and reduced ovulation. Our findings demonstrate a critical role for N-cadherin in ovarian follicular development and ovulation, and the potential to inhibit ovulation through targeting this signalling mechanism.
- 1 August 2020
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 529 (2) , 162-168
Novel N-cadherin antagonist causes glioblastoma cell death in a 3D bioprinted co-culture model
- 1 August 2020
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 529 (2) , 162-168
Novel N-cadherin antagonist causes glioblastoma cell death in a 3D bioprinted co-culture model
- Open Access
- 1 November 2010
- Published by Elsevier in Journal of Vascular Surgery
- Vol. 52 (5) , 1301-1309
Inhibition of N-cadherin retards smooth muscle cell migration and intimal thickening via induction of apoptosis
- 1 November 2010
- Published by Elsevier in Journal of Vascular Surgery
- Vol. 52 (5) , 1301-1309
Open AccessInhibition of N-cadherin retards smooth muscle cell migration and intimal thickening via induction of apoptosis
- 1 February 1995
- Published by Springer Nature in Endocrine
- Vol. 3 (2) , 83-89
Cadherins, steroids and cancer
The cadherins are a family of calcium-dependent cell adhesion molecules which are thought to be key regulators of morphogenesis. This review contains a discussion of the structure, function and regulation of these cell adhesion molecules. In particular, we discuss recent studies that demonstrate the ability of steroids to modulate cadherin levelsin vivo. We speculate that steroids and estrogenic organochlorines exert their diverse morphoregulatory actions on tissues by altering cadherin levels.
- 1 February 1995
- Published by Springer Nature in Endocrine
- Vol. 3 (2) , 83-89
Cadherins, steroids and cancer
The cadherins are a family of calcium-dependent cell adhesion molecules which are thought to be key regulators of morphogenesis. This review contains a discussion of the structure, function and regulation of these cell adhesion molecules. In particular, we discuss recent studies that demonstrate the ability of steroids to modulate cadherin levelsin vivo. We speculate that steroids and estrogenic organochlorines exert their diverse morphoregulatory actions on tissues by altering cadherin levels.