Arockia Jeyaprakash Arulanandam

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Ludwig-Maximilians-Universität München
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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

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2024

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2024

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2024

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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

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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

SPAIN
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Marin Barisic

Associate Professor

University of Copenhagen

DENMARK
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Thomas Kucharski

McGill University

CANADA
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Patrick Heun

Professor for Molecular Genetics

Technische Universität Darmstadt

GERMANY
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Tony Ly

-

UNITED KINGDOM
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Professor Keith Matthews FRS FMedSci FRSE

Professor of Parasite Biology

University of Edinburgh

UNITED KINGDOM
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Frederic Berger

Gregor Mendel Institute of Molecular Plant Biology GmbH

AUSTRIA
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Eric C. Schirmer

University of Edinburgh

UNITED KINGDOM
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Steven Shave

University of Edinburgh

UNITED KINGDOM
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Robin C Allshire

University of Edinburgh

UNITED KINGDOM
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Jakob Nilsson

Professor

University of Copenhagen

DENMARK
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Olwyn Byron

Professor of Biophysics

University of Glasgow

UNITED KINGDOM
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Kevin Hardwick

Professor of Molecular Genetics

University of Edinburgh

UNITED KINGDOM
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