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From Deworming to Cancer Therapy: Benzimidazoles in Hematological Malignancies
by
Talamo, Stella
, Golla, Upendarrao
, Shah, Nyah
, Patel, Satyam
, Claxton, David
, Sharma, Arati
, Dovat, Sinisa
, Bhalodia, Riya
in
Albendazole
/ Androgens
/ Antimitotic agents
/ Antineoplastic agents
/ Apoptosis
/ Benzimidazoles
/ Blood
/ Canada
/ Cancer
/ Cancer therapies
/ Catastrophes
/ Cell cycle
/ Cell differentiation
/ Chemotherapy
/ Clinical trials
/ Depolymerization
/ Development and progression
/ DNA damage
/ Drug approval
/ Drug development
/ Drug therapy
/ Drugs
/ FDA approval
/ Health aspects
/ Hematological diseases
/ Hematology
/ Heterozygosity
/ Kinases
/ Leukemia
/ Loss of heterozygosity
/ Lymphoma
/ Lymphomas
/ Malignancy
/ Mebendazole
/ Metabolism
/ Microtubules
/ Mortality
/ Multiple myeloma
/ Parasites
/ Physiological aspects
/ Polymerization
/ Prostate cancer
/ Proteasomes
/ Proteins
/ Review
/ Signal transduction
/ Toxicity
/ Tubulin
/ Tubulins
2024
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From Deworming to Cancer Therapy: Benzimidazoles in Hematological Malignancies
by
Talamo, Stella
, Golla, Upendarrao
, Shah, Nyah
, Patel, Satyam
, Claxton, David
, Sharma, Arati
, Dovat, Sinisa
, Bhalodia, Riya
in
Albendazole
/ Androgens
/ Antimitotic agents
/ Antineoplastic agents
/ Apoptosis
/ Benzimidazoles
/ Blood
/ Canada
/ Cancer
/ Cancer therapies
/ Catastrophes
/ Cell cycle
/ Cell differentiation
/ Chemotherapy
/ Clinical trials
/ Depolymerization
/ Development and progression
/ DNA damage
/ Drug approval
/ Drug development
/ Drug therapy
/ Drugs
/ FDA approval
/ Health aspects
/ Hematological diseases
/ Hematology
/ Heterozygosity
/ Kinases
/ Leukemia
/ Loss of heterozygosity
/ Lymphoma
/ Lymphomas
/ Malignancy
/ Mebendazole
/ Metabolism
/ Microtubules
/ Mortality
/ Multiple myeloma
/ Parasites
/ Physiological aspects
/ Polymerization
/ Prostate cancer
/ Proteasomes
/ Proteins
/ Review
/ Signal transduction
/ Toxicity
/ Tubulin
/ Tubulins
2024
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From Deworming to Cancer Therapy: Benzimidazoles in Hematological Malignancies
by
Talamo, Stella
, Golla, Upendarrao
, Shah, Nyah
, Patel, Satyam
, Claxton, David
, Sharma, Arati
, Dovat, Sinisa
, Bhalodia, Riya
in
Albendazole
/ Androgens
/ Antimitotic agents
/ Antineoplastic agents
/ Apoptosis
/ Benzimidazoles
/ Blood
/ Canada
/ Cancer
/ Cancer therapies
/ Catastrophes
/ Cell cycle
/ Cell differentiation
/ Chemotherapy
/ Clinical trials
/ Depolymerization
/ Development and progression
/ DNA damage
/ Drug approval
/ Drug development
/ Drug therapy
/ Drugs
/ FDA approval
/ Health aspects
/ Hematological diseases
/ Hematology
/ Heterozygosity
/ Kinases
/ Leukemia
/ Loss of heterozygosity
/ Lymphoma
/ Lymphomas
/ Malignancy
/ Mebendazole
/ Metabolism
/ Microtubules
/ Mortality
/ Multiple myeloma
/ Parasites
/ Physiological aspects
/ Polymerization
/ Prostate cancer
/ Proteasomes
/ Proteins
/ Review
/ Signal transduction
/ Toxicity
/ Tubulin
/ Tubulins
2024
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From Deworming to Cancer Therapy: Benzimidazoles in Hematological Malignancies
Journal Article
From Deworming to Cancer Therapy: Benzimidazoles in Hematological Malignancies
2024
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Overview
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.
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