Arockia Jeyaprakash Arulanandam
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Professor Arockia Jeyaprakash Arulanandam is a faculty member at Ludwig-Maximilians-Universität München, Germany. His primary research areas include centromere dynamics, histone modifications related to stress responses in Oryza, and the mechanisms underlying chromosome stability during cell division. His recent publications explore various aspects of spindle checkpoint signaling, centromere inheritance, and chromosomal interactions in the context of cancer and developmental syndromes.
Recent Grants
Grant: Close
Molecular Mechanisms of Centromere Inheritance and Kinetochore Function
Open Date: 2017-01-01
Close Date: 2021-12-01
Grant: Close
Molecular and structural basis for the centromeric localisation and function of the CPC in achieving faithful chromosome segregation
Open Date: 2015-01-21
Close Date: 2017-01-20
Grant: Close
Molecular and Structural Basis for the Centromeric Localisation and Function of the CPC in Achieving Faithful Chromosome Segregation
Open Date: 2015-01-01
Close Date: 2016-12-01
Grant: Close
Structural Basis for the Molecular Mechanisms Involving the Ska Complex in Establishing Stable Kinetochore-Microtubule Attachments
Open Date: 2013-04-01
Close Date: 2017-03-01
Articles (13)
Year:
2025
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2025
Year:
2024
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2024
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2024
Year:
2024
Increased nuclear size correlates with lower survival rates and higher grades for prostate cancer. The short-chain dehydrogenase/reductase (SDR) family member DHRS7 was suggested as a biomarker for use in prostate cancer grading because it is largely lost in higher-grade tumors. Here, we found that reduction in DHRS7 from the LNCaP prostate cancer cell line with normally high levels of DHRS7 increases nuclear size, potentially explaining the nuclear size increase observed in higher-grade prostate tumors where it is lost. An exogenous expression of DHRS7 in the PC3 prostate cancer cell line with normally low DHRS7 levels correspondingly decreases nuclear size. We separately tested 80 compounds from the Microsource Spectrum library for their ability to restore normal smaller nuclear size to PC3 cells, finding that estradiol propionate had the same effect as the re-expression of DHRS7 in PC3 cells. However, the drug had no effect on LNCaP cells or PC3 cells re-expressing DHRS7. We speculate that separately reported beneficial effects of estrogens in androgen-independent prostate cancer may only occur with the loss of DHRS7/ increased nuclear size, and thus propose DHRS7 levels and nuclear size as potential biomarkers for the likely effectiveness of estrogen-based treatments.
Year:
2023
Year:
2023
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2022
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2022
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2021
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2021
Year:
2020
Collaborators (13)
Anna Ruiz
Institute of Research and Innovation Parc Tauli
Marin Barisic
Associate Professor
University of Copenhagen
Thomas Kucharski
McGill University
Patrick Heun
Professor for Molecular Genetics
Technische Universität Darmstadt
Tony Ly
-
Professor Keith Matthews FRS FMedSci FRSE
Professor of Parasite Biology
University of Edinburgh
Frederic Berger
Gregor Mendel Institute of Molecular Plant Biology GmbH
Eric C. Schirmer
University of Edinburgh
Steven Shave
University of Edinburgh
Robin C Allshire
University of Edinburgh
Jakob Nilsson
Professor
University of Copenhagen
Olwyn Byron
Professor of Biophysics
University of Glasgow
Kevin Hardwick
Professor of Molecular Genetics
University of Edinburgh
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