Mebendazole as a Candidate for Drug Repurposing in Oncology: An Extensive Review of Current Literature
Open accessAbstract
Anticancer treatment efficacy is limited by the development of refractory tumor cells characterized by increased expression and activity of mechanisms promoting survival, proliferation, and metastatic spread. The present review summarizes the current literature regarding the use of the anthelmintic mebendazole (MBZ) as a repurposed drug in oncology with a focus on cells resistant to approved therapies, including so called “cancer stem cells”. Mebendazole meets many of the characteristics desirable for a repurposed drug: good and proven toxicity profile, pharmacokinetics allowing to reach therapeutic concentrations at disease site, ease of administration and low price. Several in vitro studies suggest that MBZ inhibits a wide range of factors involved in tumor progression such as tubulin polymerization, angiogenesis, pro-survival pathways, matrix metalloproteinases, and multi-drug resistance protein transporters. Mebendazole not only exhibits direct cytotoxic activity, but also synergizes with ionizing radiations and different chemotherapeutic agents and stimulates antitumoral immune response. In vivo, MBZ treatment as a single agent or in combination with chemotherapy led to the reduction or complete arrest of tumor growth, marked decrease of metastatic spread, and improvement of survival. Further investigations are warranted to confirm the clinical anti-neoplastic activity of MBZ and its safety in combination with other drugs in a clinical setting.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Because of this toxicity limitation, mebendazole rather than albendazole has been more popularly recommended as a benzimidazole anti-cancer agent.
“Because of this toxicity limitation, mebendazole rather than albendazole has been more popularly recommended as a benzimidazole anti-cancer agent [34].”
From Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update (2021) · cites this paper as [34]
The Conclusions (page unavailable) favor mebendazole as an anticancer repurposing candidate and note that higher albendazole doses were limited by neutropenia. They do not establish that mebendazole is more popularly recommended because of toxicity: the review describes albendazole’s toxicity profile as good and also cites fewer studies and less evident anticancer activity as reasons for mebendazole’s advantage. (LLM, conf=0.86)
Experimental — accuracy not yet measuredCollectively, mebendazole has been shown to not only exhibit direct cytotoxic activity, but also synergize with ionizing radiation and different chemotherapeutic agents to stimulate anti-tumoral immune responses which result in reduction or complete arrest of tumor growth, marked decrease of metastatic spread, and improvement of survival.
“Collectively, mebendazole has been shown to not only exhibit direct cytotoxic activity, but also synergize with ionizing radiation and different chemotherapeutic agents to stimulate anti-tumoral immune responses which result in reduction or complete arrest of tumor growth, marked decrease of metastatic spread, and improvement of survival [34].”
From Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update (2021) · cites this paper as [34]
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measuredMebendazole suppresses tumor growth in various cancer cell lines and animal models through inhibition of microtubule polymerization.
“MBZ has been shown to potentially suppress tumor growth in various cancer cell lines and animal models through the inhibition of microtubule polymerization”
From Drug repurposing for cancer therapy (2024) · cites this paper as [156]
Albendazole and mebendazole have been repositioned as promising anti-cancer drugs.
“It is of particular note that albendazole and mebendazole have been repositioned as promising anti-cancer drugs.”
From Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update (2021) · cites this paper as [34]
In human patients, mebendazole is contraindicated during pregnancy.
“In human patients, mebendazole is contraindicated during pregnancy [3,34].”
From Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update (2021) · cites this paper as [34]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Targeting Cancer Stemness in the Clinic: From Hype to Hope
Saygin, C., Matei, D., Majeti, R., Reizes, O., & Lathia, J. D. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2018.11.017 · Cited by 517 · cited 1× · see citing works
“Several trials testing target-therapies inhibiting a single pathway led to dismal results, likely due to the over-activation of many survival mechanism characterizing these cells [73].”
BackgroundAlbendazole, mebendazole and praziquantel. Review of non-clinical toxicity and pharmacokinetics
Dayan, A. D. (2003) · Acta Tropica · doi:10.1016/s0001-706x(03)00031-7 · Cited by 371 · see citing works
Repurposing drugs in oncology (ReDO)—Cimetidine as an anti-cancer agent
Pantziarka, P. (2014) · ecancermedicalscience · doi:10.3332/ecancer.2014.485 · Cited by 280 · see citing works
Repurposing Mebendazole as a Replacement for Vincristine for the Treatment of Brain Tumors
De Witt, M., Gamble, A., Hanson, D., Markowitz, D., Powell, C., Al Dimassi, S., Atlas, M., Boockvar, J., Ruggieri, R., & Symons, M. (2017) · Molecular Medicine · doi:10.2119/molmed.2017.00011 · Cited by 86 · see citing works
Flagged first, then by citations
Research works printed but not linked: 75
- [1]Zhao J. Cancer stem cells and chemoresistance: The smartest survives the raid Pharmacol. Ther. 2016 160 145 158 10.1016/j.pharmthera.2016.02.008 26899500 PMC4808328 · DOI
- [2]Ventola C.L. Cancer Immunotherapy, Part 3: Challenges and Future Trends Pharm. Ther. 2017 42 514 521 28781505 PMC5521300
- [3]Maeda H. Khatami M. Analyses of repeated failures in cancer therapy for solid tumors: Poor tumor-selective drug delivery, low therapeutic efficacy and unsustainable costs Clin. Transl. Med. 2018 7 11 10.1186/s40169-018-0185-6 29541939 PMC5852245 · DOI · Paper page
- [4]Zheng H.C. The molecular mechanisms of chemoresistance in cancers Oncotarget 2017 8 59950 59964 10.18632/oncotarget.19048 28938696 PMC5601792 · DOI
- [5]Wein L. Loi S. Mechanisms of resistance of chemotherapy in early-stage triple negative breast cancer (TNBC) Breast 2017 34 S27 S30 10.1016/j.breast.2017.06.023 28668293 · DOI
- [6]Velaei K. Samadi N. Barazvan B. Rad J.S. Tumor microenvironment-mediated chemoresistance in breast cancer Breast 2016 30 92 100 10.1016/j.breast.2016.09.002 27668856 · DOI
- [7]Yeldag G. Rice A. Del Río Hernández A. Chemoresistance and the Self-Maintaining Tumor Microenvironment Cancers 2018 10 471 10.3390/cancers10120471 30487436 PMC6315745 · DOI
- [8]Davis R.J. Van Waes C. Allen C.T. Overcoming barriers to effective immunotherapy: MDSCs, TAMs, and Tregs as mediators of the immunosuppressive microenvironment in head and neck cancer Oral Oncol. 2016 58 59 70 10.1016/j.oraloncology.2016.05.002 27215705 PMC4912416 · DOI
- [9]Togashi Y. Shitara K. Nishikawa H. Regulatory T cells in cancer immunosuppression - implications for anticancer therapy Nat. Rev. Clin. Oncol. 2019 16 356 371 10.1038/s41571-019-0175-7 30705439 · DOI
- [10]Vidal S.J. Rodriguez-Bravo V. Galsky M. Cordon-Cardo C. Domingo-Domenech J. Targeting cancer stem cells to suppress acquired chemotherapy resistance Oncogene 2014 33 4451 10.1038/onc.2013.411 24096485 · DOI
- [11]Scannel J.W. Diagnosing the decline in pharmaceutical R&D efficiency Nat. Rev. Drug Discov. 2012 11 191 200 22378269
- [12]Cha Y. Erez T. Reynolds I.J. Kumar D. Ross J. Koytiger G. Laifenfeld D. Zeskind B. Risso S. Kagan E. Drug repurposing from the perspective of pharmaceutical companies Br. J. Pharmacol. 2018 175 168 180 10.1111/bph.13798 28369768 PMC5758385 · DOI
- [13]WHO Informal Working Group on Echinococcosis Guidelines for treatment of cystic and alveolar echinococcosis in humans Bull. World Health Organ. 1996 74 231 242 Available online: https://www.ncbi.nlm.nih.gov/pubmed/8789923 (accessed on 30 August 2019) 8789923 PMC2486920
- [14]Todorov T. Vutova K. Mechkov G. Georgiev P. Petkov D. Tonchev Z. Nedelkov G. Chemotherapy of human cystic echinococcosis: Comparative efficacy of mebendazole and albendazole Ann. Trop Med. Parasitol. 1992 86 59 66 10.1080/00034983.1992.11812631 1616396 · DOI · Paper page
- [15]Messaritakis J. Psychou P. Nicolaidou P. Karpathios T. Syriopoulou B. Fretzayas A. Krikos F. Matsaniotis N. High mebendazole doses in pulmonary and hepatic hydatid disease Arch. Dis. Child. 1991 66 532 533 10.1136/adc.66.4.532 2031617 PMC1792968 · DOI
- [17]Fernández-Bañares F. González-Huix F. Xiol X. Catalá I. Miró J. López N. Casais L. Marrow aplasia during high dose mebendazole treatment Am. J. Trop. Med. Hyg. 1986 35 350 351 10.4269/ajtmh.1986.35.350 3953948 · DOI
- [18]Colle I. Naegels S. Hoorens A. Hautekeete M. Granulomatous hepatitis due to mebendazole J. Clin. Gastroenterol. 1999 28 44 45 10.1097/00004836-199901000-00010 9916665 · DOI · Paper page
- [19]Dawson M. Braithwaite P.A. Roberts M.S. Watson T.R. The pharmacokinetics and bioavailability of a tracer dose of [3H]-mebendazole in man Br. J. Clin. Pharmacol. 1985 19 79 86 10.1111/j.1365-2125.1985.tb02616.x 3978023 PMC1463793 · DOI
- [20]Dawson M. Allan R.J. Watson T.R. The pharmacokinetics and bioavailability of mebendazole in man: A pilot study using [3H]-mebendazole Br. J. Clin. Pharmacol. 1982 14 453 455 10.1111/j.1365-2125.1982.tb02008.x 7126419 PMC1427637 · DOI
- [21]Braithwaite P.A. Roberts M.S. Allan R.J. Watson T.R. Clinical pharmacokinetics of high dose mebendazole in patients treated for cystic hydatid disease Eur. J. Clin. Pharmacol. 1982 22 161 169 10.1007/BF00542462 7094986 · DOI
- [22]Bekhti A. Serum concentrations of mebendazole in patients with hydatid disease Int. J. Clin. Pharmacol. Ther. Toxicol. 1985 23 633 641 4093204
- [23]Corti N. Heck A. Rentsch K. Zingg W. Jetter A. Stieger B. Pauli-Magnus C. Effect of ritonavir on the pharmacokinetics of the benzimidazoles albendazole and mebendazole: An interaction study in healthy volunteers Eur. J. Clin. Pharmacol. 2009 65 999 1006 10.1007/s00228-009-0683-y 19562329 · DOI
- [24]Münst G.J. Karlaganis G. Bircher J. Plasma concentrations of mebendazole during treatment of echinococcosis: Preliminary results Eur. J. Clin. Pharmacol. 1980 17 375 378 10.1007/BF00558451 7418715 · DOI
- [26]Chico L.K. Van Eldik L.J. Watterson D.M. Targeting protein kinases in central nervous system disorders Nat. Rev. Drug Discov. 2009 8 892 909 10.1038/nrd2999 19876042 PMC2825114 · DOI
- [27]Bai R.Y. Staedtke V. Wanjiku T. Rudek M.A. Joshi A. Gallia G.L. Riggins G.J. Brain Penetration and Efficacy of Different Mebendazole Polymorphs in a Mouse Brain Tumor Model Clin. Cancer Res. 2015 21 3462 3470 10.1158/1078-0432.CCR-14-2681 25862759 PMC4526400 · DOI
- [28]Jornet D. Bosca F. Andreu J.M. Domingo L.R. Tormos R. Miranda M.A. Analysis of mebendazole binding to its target biomolecule by laser flash photolysis J. Photochem. Photobiol. B 2016 155 1 6 10.1016/j.jphotobiol.2015.12.003 26709667 · DOI
- [29]Sasaki J. Ramesh R. Chada S. Gomyo Y. Roth J.A. Mukhopadhyay T. The anthelmintic drug mebendazole induces mitotic arrest and apoptosis by depolymerizing tubulin in non-small cell lung cancer cells Mol. Cancer Ther. 2002 1 1201 1209 12479701
- [30]Bai R.Y. Staedtke V. Aprhys C.M. Gallia G.L. Riggins G.J. Antiparasitic mebendazole shows survival benefit in 2 preclinical models of glioblastoma multiforme Neuro. Oncol. 2011 13 974 982 10.1093/neuonc/nor077 21764822 PMC3158014 · DOI · Paper page
- [32]Pinto L.C. Soares B.M. Pinheiro J.D. Riggins G.J. Assumpção P.P. Burbano R.M. Montenegro R.C. The anthelmintic drug mebendazole inhibits growth, migration and invasion in gastric cancer cell model Toxicol. In Vitro 2015 29 2038 2044 10.1016/j.tiv.2015.08.007 26315676 · DOI
- [33]Mukhopadhyay T. Sasaki J. Ramesh R. Roth J.A. Mebendazole elicits a potent antitumor effect on human cancer cell lines both in vitro and in vivo Clin. Cancer Res. 2002 8 2963 2969 12231542
- [34]Northcott P.A. Jones D.T. Kool M. Robinson G.W. Gilbertson R.J. Cho Y.J. Pomeroy S.L. Korshunov A. Lichter P. Taylor M.D. Medulloblastomics: The end of the beginning Nat. Rev. Cancer. 2012 12 818 834 10.1038/nrc3410 23175120 PMC3889646 · DOI
- [35]Bai R.Y. Staedtke V. Rudin C.M. Bunz F. Riggins G.J. Effective treatment of diverse medulloblastoma models with mebendazole and its impact on tumor angiogenesis Neuro. Oncol. 2015 17 545 554 10.1093/neuonc/nou234 25253417 PMC4483072 · DOI
- [36]Williamson T. Bai R.Y. Staedtke V. Huso D. Riggins G.J. Mebendazole and a non-steroidal anti-inflammatory combine to reduce tumor initiation in a colon cancer preclinical model Oncotarget 2016 7 68571 68584 10.18632/oncotarget.11851 27612418 PMC5356574 · DOI
- [37]Sung S.J. Kim H.K. Hong Y.K. Joe Y.A. Autophagy Is a Potential Target for Enhancing the Anti-Angiogenic Effect of Mebendazole in Endothelial Cells Biomol. Ther. 2019 27 117 125 10.4062/biomolther.2018.222 PMC6319545 30642153 · DOI
- [38]Amakye D. Jagani Z. Dorsch M. Unraveling the therapeutic potential of the Hedgehog pathway in cancer Nat. Med. 2013 19 1410 1422 10.1038/nm.3389 24202394 · DOI
- [39]Larsen A.R. Bai R.Y. Chung J.H. Borodovsky A. Rudin C.M. Riggins G.J. Bunz F. Repurposing the antihelmintic mebendazole as a hedgehog inhibitor Mol. Cancer Ther. 2015 14 3 13 10.1158/1535-7163.MCT-14-0755-T 25376612 PMC4297232 · DOI
- [40]Hiscutt E.L. Hill D.S. Martin S. Kerr R. Harbottle A. Lovat P.E. Redfern C.P. Fulda S. Armstrong J.L. Lovat P.E. Targeting X-linked inhibitor of apoptosis protein to increase the efficacy of endoplasmic reticulum stress-induced apoptosis for melanoma therapy J. Investig. Dermatol. 2010 130 2250 2258 10.1038/jid.2010.146 20520630 · DOI
- [41]Doudican N.A. Byron S.A. Pollock P.M. Orlow S.J. XIAP downregulation accompanies mebendazole growth inhibition in melanoma xenografts Anticancer Drugs 2013 24 181 188 10.1097/CAD.0b013e32835a43f1 23059386 · DOI
- [42]Wan P.T. Garnett M.J. Roe S.M. Lee S. Niculescu-Duvaz D. Good V.M. Jones C.M. Marshall C.J. Springer C.J. Barford D. Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF Cell 2004 116 855 867 10.1016/S0092-8674(04)00215-6 15035987 · DOI
- [43]Simbulan-Rosenthal C.M. Dakshanamurthy S. Gaur A. Chen Y.S. Fang H.B. Abdussamad M. Zhou H. Zapas J. Calvert V. Petricoin E.F. The repurposed anthelmintic mebendazole in combination with trametinib suppresses refractory NRASQ61K melanoma Oncotarget 2017 8 12576 12595 10.18632/oncotarget.14990 28157711 PMC5355037 · DOI
- [44]Fry E.A. Inoue K. C-MYB and DMTF1 in Cancer Cancer Investig. 2019 37 46 65 10.1080/07357907.2018.1550090 30599775 PMC6431554 · DOI
- [45]Walf-Vorderwülbecke V. Pearce K. Brooks T. Hubank M. van den Heuvel-Eibrink M.M. Zwaan C.M. Adams S. Edwards D. Bartram J. Samarasinghe S. Targeting acute myeloid leukemia by drug-induced c-MYB degradation Leukemia. 2018 32 882 889 10.1038/leu.2017.317 29089643 · DOI
- [46]Joyce H. McCann A. Clynes M. Larkin A. Influence of multidrug resistance and drug transport proteins on chemotherapy drug metabolism Expert Opin. Drug Metab. Toxicol. 2015 11 795 809 10.1517/17425255.2015.1028356 25836015 · DOI
- [47]Celestino Pinto L. de Fátima Aquino Moreira-Nunes C. Soares B.M. Burbano R.M.R. de Lemos J.A.R. Montenegro R.C. Mebendazole, an antiparasitic drug, inhibits drug transporters expression in preclinical model of gastric peritoneal carcinomatosis Toxicol. In Vitro 2017 43 87 91 10.1016/j.tiv.2017.06.007 28606429 · DOI
- [48]Kralova V. Hanušová V. Caltová K. Špaček P. Hochmalová M. Skálová L. Rudolf E. Flubendazole and mebendazole impair migration and epithelial to mesenchymal transition in oral cell lines Chem. Biol. Interact. 2018 293 124 132 30075109
- [49]Poruchynsky M. Komlodi-Pasztor E. Trostel S. Wilkerson J. Regairaz M. Pommier Y. Zhang X. Kumar M.T. Robey R. Burotto M. Microtubule-targeting agents augment the toxicity of DNA-damaging agents by disrupting intracellular trafficking of DNA repair proteins Proc. Natl. Acad. Sci. USA 2015 112 1571 1576 25605897 PMC4321245
- [50]Markowitz D. Ha G. Ruggieri R. Symons M. Microtubule-targeting agents can sensitize cancer cells to ionizing radiation by an interphase-based mechanism Onco. Targets Ther. 2017 10 5633 5642 10.2147/OTT.S143096 29200877 PMC5703169 · DOI
- [51]Zhang L. Bochkur D.M. Yazal T. Dong K. Nguyen A. Yu G. Dao A. Bochkur D.M. Duhachek-Muggy S. Bhat K. Mebendazole Potentiates Radiation Therapy in Triple-Negative Breast Cancer Int. J. Radiat. Oncol. Biol. Phys. 2019 103 195 207 10.1016/j.ijrobp.2018.08.046 30196056 PMC6457649 · DOI
- [52]Coyne C.P. Jones T. Bear R. Anti-Neoplastic Cytotoxicity of Gemcitabine-(C4-amide)-[anti-EGFR] in Dual-combination with Epirubicin-(C3-amide)-[anti-HER2/neu] against Chemotherapeutic-Resistant Mammary Adenocarcinoma (SKBr-3) and the Complementary Effect of Mebendazole J. Cancer Res. Ther. Oncol. 2014 2 203 10.17303/jcrto.2014.203 25844392 PMC4381351 · DOI
- [53]Kipper F.C. Silva A.O. Marc A.L. Confortin G. Junqueira A.V. Neto E.P. Lenz G. Vinblastine and antihelmintic mebendazole potentiate temozolomide in resistant gliomas Investig. New Drugs. 2018 36 323 331 10.1007/s10637-017-0503-7 28852916 · DOI
- [54]Buttrick S. Shah A.H. Komotar R.J. Ivan M.E. Management of Atypical and Anaplastic Meningiomas Neurosurg. Clin. N. Am. 2016 27 239 247 10.1016/j.nec.2015.11.003 27012388 · DOI
- [55]Skibinski C.G. Williamson T. Riggins G.J. Mebendazole and radiation in combination increase survival through anticancer mechanisms in an intracranial rodent model of malignant meningioma J. Neurooncol. 2018 140 529 538 10.1007/s11060-018-03009-7 30414098 PMC6387633 · DOI
- [56]Zhang F. Li Y. Zhang H. Huang E. Gao L. Luo W. Wei Q. Fan J. Song D. Liao J. Anthelmintic Mebendazole enhances cisplatin’s effect on suppressing cell proliferation and promotes differentiation of head and neck squamous cell carcinoma (HNSCC) Oncotarget 2017 8 12968 12982 28099902 PMC5355070
- [57]Martarelli D. Pompei P. Baldi C. Mazzoni G. Mebendazole inhibits growth of human adrenocortical carcinoma cell lines implanted in nude mice Cancer Chemother. Pharmacol. 2008 61 809 817 10.1007/s00280-007-0538-0 17581752 · DOI · Paper page
- [58]Doudican N. Rodriguez A. Osman I. Orlow S.J. Mebendazole induces apoptosis via Bcl-2 inactivation in chemoresistant melanoma cells Mol. Cancer Res. 2008 6 1308 1315 10.1158/1541-7786.MCR-07-2159 18667591 · DOI · Paper page
- [59]Pinto L.C. Mesquita F.P. Soares B.M. da Silva E.L. Puty B. de Oliveira E.H. Burbano R.R. Montenegro R.C. Mebendazole induces apoptosis via C-MYC inactivation in malignant ascites cell line (AGP01) Toxicol. In Vitro 2019 60 305 312 10.1016/j.tiv.2019.06.010 31207347 · DOI
- [60]Dakshanamurthy S. Issa N.T. Assefnia S. Seshasayee A. Peters O.J. Madhavan S. Uren A. Brown M.L. Byers S.W. Predicting New Indications for Approved Drugs Using a Proteo-Chemometric Method J. Med. Chem. 2012 55 6832 6848 10.1021/jm300576q 22780961 PMC3419493 · DOI
- [61]Issa N.T. Peters O.J. Byers S.W. Dakshanamurthy S. Repurpose VS: A Drug Repurposing-Focused Computational Method for Accurate Drug-Target Signature Predictions Comb. Chem. High. Throughput Screen 2015 18 784 794 10.2174/1386207318666150803130138 26234515 PMC5848469 · DOI
- [62]Yamada T. Masuda M. Emergence of TNIK inhibitors in cancer therapeutics Cancer Sci. 2017 108 818 823 10.1111/cas.13203 28208209 PMC5448614 · DOI
- [63]Tan Z. Chen L. Zhang S. Comprehensive Modeling and Discovery of Mebendazole as a Novel TRAF2- and NCK interacting Kinase Inhibitor Sci. Rep. 2016 6 33534 10.1038/srep33534 27650168 PMC5030704 · DOI
- [64]Nygren P. Fryknäs M. Agerup B. Larsson R. Repositioning of the anthelmintic drug mebendazole for the treatment for colon cancer J. Cancer Res. Clin. Oncol. 2013 139 2133 2140 10.1007/s00432-013-1539-5 24135855 PMC3825534 · DOI · Paper page
- [65]Aras S. Zaidi M.R. TAMeless traitors: Macrophages in cancer progression and metastasis Br. J. Cancer 2017 117 1583 1591 10.1038/bjc.2017.356 29065107 PMC5729447 · DOI
- [66]Blom K. Senkowski W. Jarvius M. Berglund M. Rubin J. Larsson R. The anticancer effect of mebendazole may be due to M1 monocyte/macrophage activation via ERK1/2 and TLR8-dependent inflammasome activation Immunopharmacol. Immunotoxicol. 2017 39 199 210 10.1080/08923973.2017.1320671 28472897 · DOI
- [67]Rubin J. Mansoori S. Blom K. Berglund M. Lenhammar L. Andersson C. Loskog A. Fryknäs M. Nygren P. Larsson R. Mebendazole stimulates CD14+ myeloid cells to enhance T-cell activation and tumour cell killing Oncotarget 2018 9 30805 30813 10.18632/oncotarget.25713 30112108 PMC6089388 · DOI
- [68]Blom K. Rubin J. Berglund M. Jarvius M. Lenhammar L. Parrow V. Andersson C. Loskog A. Fryknäs M. Nygren P. Mebendazole-induced M1 polarization of THP-1 macrophages may involve DYRK1B inhibition BMC Res. Notes 2019 12 234 10.1186/s13104-019-4273-5 31010428 PMC6477744 · DOI
- [69]Dobrosotskaya I.Y. Hammer G.D. Schteingart D.E. Maturen K.E. Worden F.P. Mebendazole monotherapy and long-term disease control in metastatic adrenocortical carcinoma Endocr. Pract. 2011 17 e59 e62 10.4158/EP10390.CR 21454232 · DOI · Paper page
- [70]Nygren P. Larsson R. Drug repositioning from bench to bedside: Tumour remission by the antihelmintic drug mebendazole in refractory metastatic colon cancer Acta. Oncol. 2014 53 427 428 10.3109/0284186X.2013.844359 24160353 · DOI · Paper page
- [72]Nair A.B. Jacob S. A simple practice guide for dose conversion between animals and human J. Basic Clin. Pharm. 2016 7 27 31 10.4103/0976-0105.177703 27057123 PMC4804402 · DOI · Paper page
- [74]Sasagawa S. Nishimura Y. Kon T. Yamanaka Y. Kawase R. Tanaka T. DNA Damage Response Is Involved in the Developmental Toxicity of Mebendazole in Zebrafish Retina Front. Pharmacol. 2016 7 57 10.3389/fphar.2016.00057 27014071 PMC4789406 · DOI
- [75]Gillies R.J. Verduzco D. Gatenby R. Evolutionary dynamics of carcinogenesis and why targeted therapy does not work Nat. Rev. Cancer 2012 12 487 493 10.1038/nrc3298 22695393 PMC4122506 · DOI
- [76]Lien K. Georgsdottir S. Sivanathan L. Chan K. Emmenegger U. Low-dose metronomic chemotherapy: A systematic literature analysis Eur. J. Cancer 2013 49 3387 3395 10.1016/j.ejca.2013.06.038 23880474 · DOI
- [77]Bertolini F. Sukhatme V.P. Bouche G. Drug repurposing in oncology--patient and health systems opportunities Nat. Rev. Clin. Oncol. 2015 12 732 742 10.1038/nrclinonc.2015.169 26483297 · DOI
- [78]Pantziarka P. Bouche G. Meheus L. Sukhatme V. Sukhatme V.P. Vikas P. The Repurposing Drugs in Oncology (ReDO) Project Ecancermedicalscience 2014 8 442 10.3332/ecancer.2014.485 25075216 PMC4096030 · DOI · Paper page
- [79]Arif S.H. Shams-Ul-Bari Wani N.A. Zargar S.A. Wani M.A. Tabassum R. Hussain Z. Baba A.A. Lone R.A. Albendazole as an adjuvant to the standard surgical management of hydatid cyst liver Int. J. Surg. 2008 6 448 451 10.1016/j.ijsu.2008.08.003 18819855 · DOI
- [80]Pourgholami M.H. Szwajcer M. Chin M. Liauw W. Seef J. Galettis P. Morris D.L. Links M. Phase I clinical trial to determine maximum tolerated dose of oral albendazole in patients with advanced cancer Cancer Chemother. Pharmacol. 2010 65 597 605 10.1007/s00280-009-1157-8 19904538 · DOI · Paper page
Cited by
Sorted by citations
Drug repurposing for cancer therapy
Xia, Y., Sun, M., Huang, H., & Jin, W.-L. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01808-1 · Cited by 443 · see citing works
Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update
Chai, J.-Y., Jung, B.-K., & Hong, S.-J. (2021) · The Korean Journal of Parasitology · doi:10.3347/kjp.2021.59.3.189 · Cited by 286 · see citing works
Fu, L., Jin, W., Zhang, J., Zhu, L., Lu, J., Zhen, Y., Zhang, L., Ouyang, L., Liu, B., & Yu, H. (2022) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.09.006 · Cited by 83 · see citing works
Limbu, K. R., Chhetri, R. B., Oh, Y. S., Baek, D. J., & Park, E.-Y. (2022) · Molecules · doi:10.3390/molecules27238127 · Cited by 12 · see citing works
Joe, N. S., Wang, Y., Oza, H. H., Godet, I., Milki, N., Riggins, G. J., & Gilkes, D. M. (2023) · Cancers · doi:10.3390/cancers15041330 · Cited by 9 · see citing works
- Authors
- Guerini, A. E., Triggiani, L., Maddalo, M., Bonù, M. L., Frassine, F., Baiguini, A., Alghisi, A., Tomasini, D., Borghetti, P., Pasinetti, N., Bresciani, R., Magrini, S. M., & Buglione, M.
- Affiliations
- University of Brescia (IT)
- Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia (IT)
- Aziende Socio Sanitarie Territoriale della Valcamonica (IT)
- Corresponding author
- Maddalo, Marta
- Tomasini, Davide
- ORCID
- Venue
- Cancers
- Publisher
- MDPI AG
- Published
- 2019-08-31
- Volume
- 11
- Issue
- 9
- Pages
- 1284
- ISSN
- 2072-6694 (ISSN-L)
- PMC
- PMC6769799
- OpenAlex
- W2971269332
- Cited by
- 146
- References
- 4
- Citations by year
- 2026: 11 · 2025: 21 · 2024: 18 · 2023: 26 · 2022: 33 · 2021: 26 · 2020: 10 · 2019: 1
- FWCI
- 1.67
- Type
- journal article
- Language
- en
- Open access
- gold
- dx.doi.org
- Licence
- Locations
- Cancers (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Institutional Research Information System (Università degli Studi di Brescia) (submittedVersion, public-domain)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Health Sciences › Medicine › Pathology and Forensic Medicine › Cancer Mechanisms and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cancer therapeutics and mechanisms
- Keywords
- mebendazole, drug repurposing, cancer stem cells, drug resistance, tubulin polymerization inhibition, angiogenesis inhibition, matrix metalloproteinases, multidrug resistance transporters, radiosensitization, chemosensitization, antitumor immunity, metastasis, combination chemotherapy
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review