Evidence map›Paper›PMID 40712054›Full record

ArticleCancer research2025

Carbonic Anhydrase Inhibition Sensitizes Group 3 Medulloblastoma to Radiotherapy.

Cory M Richman, Alexandra Rasnitsyn, Borja L Holgado, Maria Vladoiu, Namal Abeysundara, Sandra Majo, Sara Chabi, Lucie J Taunay, Hiromichi Suzuki, Ichiyo Shibahara and 21 more

Abstract read
In one paragraph

Article in Cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

31 authors.

Cory M RichmanThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0009-0003-0321-4696
Alexandra RasnitsynThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0009-0002-8491-6763
Borja L HolgadoThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0009-0005-7926-3990
Maria VladoiuThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0000-0001-8644-0581
Namal AbeysundaraThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0009-0009-9386-1240
Sandra MajoInstitut Curie, CNRS UMR3347, INSERM U1021, University UPSaclay, PSL, Equipe Labellisée Ligue Contre le Cancer, Centre Universitaire, Orsay, France.ORCID 0009-0004-1976-9167
Sara ChabiInstitut Curie, CNRS UMR3347, INSERM U1021, University UPSaclay, PSL, Equipe Labellisée Ligue Contre le Cancer, Centre Universitaire, Orsay, France.ORCID 0009-0001-4629-103X
Lucie J TaunayInstitut Curie, CNRS UMR3347, INSERM U1021, University UPSaclay, PSL, Equipe Labellisée Ligue Contre le Cancer, Centre Universitaire, Orsay, France.ORCID 0009-0001-8924-5586
Hiromichi SuzukiDivision of Brain Tumor Translational Research, National Cancer Center Research Institute, Tokyo, Japan.ORCID 0000-0002-8858-0294
Ichiyo ShibaharaDepartment of Neurosurgery, Kitasato University School of Medicine, Sagamihara, Japan.ORCID 0000-0001-6453-0076
Joonas HaapasaloThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0000-0002-6468-4937
Jonelle G PallottaThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0009-0000-1593-8577
Tajana DouglasThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0009-0000-4243-231X
Kaitlin KharasThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0000-0001-7834-7061
Kyle JuraschkaThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0000-0002-9549-9224
Oliver OcsenasDepartment of Medical Biophysics, University of Toronto, Toronto, Canada.ORCID 0009-0001-2543-5014
Sachin A KumarThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0000-0002-4853-3864
Kristiina NordforsThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0000-0002-3680-4524
Ana Guerreiro StücklinThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0000-0003-3136-9241
Raul A SuarezThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0009-0003-4531-9656
Jiao ZhangTexas Children's Cancer and Hematology Center, Houston, Texas.ORCID 0000-0001-8218-3688
Xiaochong WuTexas Children's Cancer and Hematology Center, Houston, Texas.ORCID 0009-0000-9896-5967
Craig DanielsTexas Children's Cancer and Hematology Center, Houston, Texas.ORCID 0009-0005-1614-6682
Livia GarziaCancer Research Program, McGill University Health Centre Research Institute, Montreal, Canada.ORCID 0000-0002-5016-0753
Jüri ReimandDepartment of Medical Biophysics, University of Toronto, Toronto, Canada.ORCID 0000-0002-2299-2309
Olivier SaulnierThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0000-0003-4111-1017
Thomas E MerchantDepartment of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0002-0412-6255
Celio PouponnotInstitut Curie, CNRS UMR3347, INSERM U1021, University UPSaclay, PSL, Equipe Labellisée Ligue Contre le Cancer, Centre Universitaire, Orsay, France.ORCID 0000-0002-9795-0496
David R RaleighDepartment of Radiation Oncology, University of California San Francisco, San Francisco, California.ORCID 0000-0001-9299-8864
Michael D TaylorThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0000-0001-7009-3466
Pasqualino De AntonellisThe Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.ORCID 0000-0001-8551-9431

Funding

Mouse models to discover new drivers of medulloblastomaR01CA159859 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI Michael D. Taylor, WILLIAM A WEISS · 2011 to 2026
$10.4M
CCL2 and CCR2 as metastatic drivers and therapeutic targets in medulloblastomaR01CA255369 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GARZIA, LIVIA, TAYLOR, MICHAEL D. · 2021 to 2025
$3.9M
Prevention and treatment of lethal metastases in group 3 medulloblastomaR01NS106155 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TAYLOR, MICHAEL D., WEISS, WILLIAM A · 2018 to 2022
$2.8M
All of Us Research Program (AoURP) R01CA159859All of Us Research Program (AoURP) R01CA255369All of Us Research Program (AoURP) R01NS106155Cancer Prevention and Research Institute of Texas (CPRIT) RR220051Fondazione AIRC per la ricerca sul cancro ETS (AIRC) 17881NCI NIH HHS R01 CA159859NCI NIH HHS R01 CA255369NINDS NIH HHS R01 NS106155Stand Up To Cancer Canada (SU2C Canada) SU2C-AACR-DT1113Stand Up To Cancer (SU2C) SU2C-AACR-DT-19-15
6 · The paper itself

Abstract

Group 3 (G3) medulloblastoma constitutes the most aggressive molecular subgroup, and nearly all patients present with metastases upon recurrence. Treatment for newly diagnosed medulloblastoma relies on a combination of maximal safe surgical resection, followed by chemotherapy and ionizing radiation, and no therapies have been shown to confer a survival benefit at the time of recurrence. Given the limited therapeutic options available for patients with medulloblastoma, especially at recurrence, and the incomplete understanding of the molecular mechanisms underlying resistance to treatment, we sought to uncover actionable targets and biomarkers that could help refine patient selection and treatment of newly diagnosed medulloblastoma to reduce the risk of recurrence. In clinically relevant mouse models of G3 medulloblastoma, CT-guided fractionated radiotherapy extended overall survival and induced the clonal selection of radioresistant subpopulations of tumor cells that drove medulloblastoma recurrence. Comparison of recurrent tumors with treatment-naïve newly diagnosed tumors revealed a gene expression signature that was found to be a biomarker of radioresistance and poor prognosis. This prognostic gene signature was shown to be subgroup specific in a large patient cohort. Recurrent tumors had elevated expression of carbonic anhydrase 4, and genetic and pharmacologic modulation of carbonic anhydrase 4 could promote or reduce resistance to radiotherapy. These data suggest that the FDA-approved carbonic anhydrase inhibitor acetazolamide may be a useful radiosensitizer to improve the efficacy of the treatment of newly diagnosed G3 medulloblastoma that could reduce the risk of tumor recurrence and improve survival in pediatric patients. SIGNIFICANCE: G3 medulloblastoma features a prognostic subgroup-specific gene expression signature and can be targeted with a carbonic anhydrase inhibitor to enhance radiosensitivity, reducing the risk of recurrence and improving survival.

Indexed as

Carbonic Anhydrase InhibitorsCerebellar NeoplasmsMedulloblastomaNeoplasm Recurrence, LocalRadiation ToleranceAnimalsBiomarkers, TumorFemaleHumansMicePrognosisXenograft Model Antitumor AssaysBiomarkers, TumorCarbonic Anhydrase Inhibitors

Identifiers

PMID40712054
PMCPMC12442109

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.