Evidence map›Paper›PMID 39456548›Full record

ReviewCancers2024

From Deworming to Cancer Therapy: Benzimidazoles in Hematological Malignancies.

Upendarrao Golla, Satyam Patel, Nyah Shah, Stella Talamo, Riya Bhalodia, David Claxton, Sinisa Dovat, Arati Sharma

Abstract readReview
In one paragraph

Review in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
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

8 authors.

Upendarrao GollaDivision of Hematology and Oncology, Department of Medicine, Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.ORCID 0000-0003-0519-7087
Satyam PatelDepartment of Pharmacology, Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.ORCID 0000-0003-1578-2749
Nyah ShahDepartment of Health Sciences, McMaster University, Hamilton, ON L8S 4L8, Canada.ORCID 0000-0001-9987-7678
Stella TalamoDepartment of Medicine, Liberty University College of Osteopathic Medicine, Lynchburg, VA 24502, USA.
Riya BhalodiaDivision of Hematology and Oncology, Department of Pediatrics, Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.ORCID 0000-0003-1932-3937
David ClaxtonDivision of Hematology and Oncology, Department of Medicine, Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.
Sinisa DovatDivision of Hematology and Oncology, Department of Pediatrics, Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.
Arati SharmaPenn State Cancer Institute, Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.

Funding

Novel targeted therapy to reduce health disparities in pediatric leukemiaR01CA278226 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI Sinisa Dovat · 2023 to 2026
$2.1M
NCI NIH HHS R01 CA278226
6 · The paper itself

Abstract

Drug repurposing is a strategy to discover new therapeutic uses for existing drugs, which have well-established toxicity profiles and are often more affordable. This approach has gained significant attention in recent years due to the high costs and low success rates associated with traditional drug development. Drug repositioning offers a more time- and cost-effective path for identifying new treatments. Several FDA-approved non-chemotherapy drugs have been investigated for their anticancer potential. Among these, anthelmintic benzimidazoles (such as albendazole, mebendazole, and flubendazole) have garnered interest due to their effects on microtubules and oncogenic signaling pathways. Blood cancers, which frequently develop resistance and have high mortality rates, present a critical need for effective therapies. This review highlights the recent advances in repurposing benzimidazoles for blood malignancies. These compounds induce cell cycle arrest, differentiation, tubulin depolymerization, loss of heterozygosity, proteasomal degradation, and inhibit oncogenic signaling to exert their anticancer effects. We also discuss current limitations and strategies to overcome them, emphasizing the potential of combining benzimidazoles with standard therapies for improved treatment of hematological cancers.

Indexed as

anthelminticapoptosisbenzimidazole derivativescancerdifferentiation therapydrug repurposeleukemialymphomasignaling pathwaystubulin polymerization

Identifiers

PMID39456548
PMCPMC11506385

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.