Jos Jonkers
@josjonkers.bsky.social
📤 86
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Breast cancer researcher at the Netherlands Cancer Institute
reposted by
Jos Jonkers
Barbara Marte
about 1 month ago
new out in Nature
www.nature.com/articles/s41...
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Axonal injury is a targetable driver of glioblastoma progression - Nature
Axonal injury, induced in the white matter by expansion of early tumour cells, is a key driver of glioblastoma progression.
https://www.nature.com/articles/s41586-025-09411-2
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reposted by
Jos Jonkers
Netherlands Cancer Institute
about 1 month ago
Breaking the chain: uncovering a hidden weakness in PARP-resistant cancers ➡️
www.nki.nl/news-events/...
#fundamentalresearch
#cancerresearch
#NKI
#breastcancer
#ovariancancer
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reposted by
Jos Jonkers
ByteTrending
about 1 month ago
NASP Funding: Maximize Your Program’s Impact Researchers discovered that NASP, a key protein involved in chromatin organization, plays a surprising role in resistance to PARP inhibitors. Targeting NASP offers a new therapeutic strategy for cancer treatment.
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NASP Funding: Maximize Your Program’s Impact
Researchers discovered that NASP, a key protein involved in chromatin organization, plays a surprising role in resistance to PARP inhibitors. Targeting NASP offers a new therapeutic strategy for cancer treatment.
https://bytetrending.com/2025/08/16/nasp-funding-maximize-your-programs-impact/?utm_source=bluesky&utm_medium=jetpack_social
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reposted by
Jos Jonkers
Nature
about 1 month ago
Nature research paper: NASP modulates histone turnover to drive PARP inhibitor resistance
go.nature.com/45vRWhd
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NASP modulates histone turnover to drive PARP inhibitor resistance - Nature
PARP inhibitor treatment triggers histone release from the chromatin in cancer cells; consequently, targeting the histone chaperone NASP renders cells vulnerable to PARP inhibition.
https://go.nature.com/45vRWhd
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reposted by
Jos Jonkers
Sarah Moser
about 1 month ago
Thrilled to share our latest work, just published in
@nature.com
⬇
www.nature.com/articles/s41...
We discovered that PARP inhibitors đź’Š trigger histone eviction from the chromatin and this creates a hidden vulnerability in PARPi resistant tumors. đź§µ (1/8)
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NASP modulates histone turnover to drive PARP inhibitor resistance - Nature
PARP inhibitor treatment triggers histone release from the chromatin in cancer cells; consequently, targeting the histone chaperone NASP renders cells vulnerable to PARP inhibition.
https://www.nature.com/articles/s41586-025-09414-z
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reposted by
Jos Jonkers
Barbara Marte
about 1 month ago
new out in Nature yesterday
www.nature.com/articles/s41...
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NASP modulates histone turnover to drive PARP inhibitor resistance - Nature
PARP inhibitor treatment triggers histone release from the chromatin in cancer cells; consequently, targeting the histone chaperone NASP renders cells vulnerable to PARP inhibition.
https://www.nature.com/articles/s41586-025-09414-z
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reposted by
Jos Jonkers
Craig Kaplan
about 1 month ago
Extremely cool!
add a skeleton here at some point
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reposted by
Jos Jonkers
Abdel Mazouzi
about 1 month ago
I am thrilled to share with you my first co-corresponding author Nature paper with Jos Jonkers. This project was led by the extraordinary
@sarahmoser.bsky.social
. Congratulations, and thank you to all the authors,
@nkinl.bsky.social
, and
@oncodeinstitute.bsky.social
for their support.
add a skeleton here at some point
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reposted by
Jos Jonkers
Sarah Moser
about 1 month ago
This project has been a truly exciting chapter of my PhD journey and I am deeply grateful to everyone involved. A heartfelt thank you to my mentors,
@josjonkers.bsky.social
and
@amazouzi.bsky.social
for their guidance in solving the histone puzzle.
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reposted by
Jos Jonkers
SCIENMAG
about 1 month ago
NASP Controls Histone Turnover Behind PARP Resistance The emergence of poly(ADP-ribose) polymerase inhibitors (PARPi) as a transformative therapy for homologous recombination-deficient tumors has significantly altered the landscape of cancer treatment. These drugs exploit synthetic lethality to…
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NASP Controls Histone Turnover Behind PARPÂ Resistance
The emergence of poly(ADP-ribose) polymerase inhibitors (PARPi) as a transformative therapy for homologous recombination-deficient tumors has significantly altered the landscape of cancer treatment. These drugs exploit synthetic lethality to selectively kill tumor cells harboring defects in DNA repair pathways, particularly BRCA1 and BRCA2 mutations. However, the clinical utility of PARPi is frequently hampered by the development of resistance, posing a formidable challenge for long-term therapeutic success.
https://scienmag.com/nasp-controls-histone-turnover-behind-parp-resistance/?utm_source=bluesky&utm_medium=jetpack_social
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