The DOI matches its Crossref record.
Taxanes: Microtubule and Centrosome Targets, and Cell Cycle Dependent Mechanisms of Action
Abstract
Microtubules are highly dynamic cellular polymers made of alphabeta-tubulin and associated proteins. They play a key role during mitosis, participating in the exact organization and function of the spindle, and are critical for assuring the integrity of the segregated DNA. Therefore, they represent one of the more effective targets in current cancer therapy. Paclitaxel (Taxol) is the prototype of the taxane family of antitumor drugs, and it was the first natural product shown to stabilize microtubules. This unique mechanism of action is in contrast to other microtubule poisons, such as Vinca alkaloids, colchicine, and cryptophycines, which inhibit tubulin polymerization. Taxanes block cell cycle progression through centrosomal impairment, induction of abnormal spindles and suppression of spindle microtubule dynamics. Triggering of apoptosis by aberrant mitosis or by subsequent multinucleated G1-like state related to mitotic slippage, depends on cell type and drug schedule. The development of fluorescent derivatives of paclitaxel led us to locate spindle pole microtubules and centrosomes as main sub-cellular targets of cytotoxic taxoids in living cells. In this review we discuss these findings in the context of a cell cycle-dependent response to taxanes, based on the cellular targets, and the status of the implicated cell cycle checkpoints. We also review those events that can influence this response, like the different signal transduction pathways activated/inactivated in relation to Bcl-2 phosphorylation and induction of apoptosis, and the controversial role of the p53 status on cell sensitivity to paclitaxel. Finally, cell cycle-dependent resistance, an emerging concept in combination sequential chemotherapy, is discussed on the basis of the cell cycle-dependent mechanisms of action of taxanes.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“Taxanes act by stabilizing the link between individual tubulin dimmers [21].”
From Chemotherapeutic treatment efficacy and sensitivity are increased by adjuvant alternating electric fields (TTFields) (2009) · cites this paper as [21]
In the citing paper
“In the specific case of Paclitaxel, one of the most commonly used treatments for late-stage human breast cancer [20], the combined effect may be attributed to their similar site of action – the spindle microtubules [1,2,21].”
From Chemotherapeutic treatment efficacy and sensitivity are increased by adjuvant alternating electric fields (TTFields) (2009) · cites this paper as [21]
In the citing paper
“As illustrated schematically in Figure 7A taxanes increase the length of tubulin filaments within the cell.”
From Chemotherapeutic treatment efficacy and sensitivity are increased by adjuvant alternating electric fields (TTFields) (2009) · cites this paper as [21]
Citations
Cited by
Sorted by citations
Items 101–200 of 384
Ceramella, J., Caruso, A., Occhiuzzi, M. A., et al. (2019) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2019.111583 · Cited by 44
Novel indication for cancer therapy: Chk1 inhibition sensitizes tumor cells to antimitotics
Xiao, Z., Xue, J., Semizarov, D., Sowin, T. J., Rosenberg, S. H., & Zhang, H. (2005) · International Journal of Cancer · doi:10.1002/ijc.20770 · Cited by 44
“It induces the spindle checkpoint through suppression of spindle microtubule dynamics by binding to the b-subunit of tubulin and stabilizing microtubules.(4,5) The resultant mitotic arrest will trigger rapid onset of p53-independent apoptotic pathway.”
BackgroundZhang, X., Ling, M., Wang, X., et al. (2005) · International Journal of Cancer · doi:10.1002/ijc.21592 · Cited by 44
“It is well established that taxol interferes with microtubules and induces G2/M arrest, which in turn, triggers apoptosis.(21,22) However, G2/M-independent apoptosis has also been reported.”
BackgroundHan, G., Liu, Z., Shimoi, K., et al. (2005) · Cancer Research · doi:10.1158/0008-5472.387.65.2 · Cited by 43
Photodynamic therapy induced cell cycle arrest and cancer cell synchronization: review
Moloudi, K., Abrahamse, H., & George, B. P. A. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1225694 · Cited by 45
A Systematic Review on Antitumor Agents with 1, 3, 5-triazines
Liu, B. (2015) · Medicinal Chemistry · doi:10.4172/2161-0444.1000255 · Cited by 42
“Although the range of antimitotic agent is extremely large, only few agents received clinical and commercial success up to present [134-139].”
BackgroundFormulation of Acid-Sensitive Micelles for Delivery of Cabazitaxel into Prostate Cancer Cells
Aydin, Ö. F., Youssef, I., Durmaz, Y. Y., Tiruchinapally, G., & ElSayed, M. E. H. (2016) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.6b00147 · Cited by 42
Dijkhuis, A., Klappe, K., Jacobs, S. C., et al. (2006) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-05-0457 · Cited by 42
“At high paclitaxel concentrations, bipolar spindle formation is affected possibly due to an additional effect of paclitaxel on centrosome function (3).”
BackgroundTulsyan, S., Chaturvedi, P. K., Singh, A. K., et al. (2014) · Gene · doi:10.1016/j.gene.2014.04.004 · Cited by 41
“Paclitaxel and docetaxel — the two common taxanes interfere with themicrotubules at themitotic spindle, resulting in cell cycle arrest duringmitosis and finally cell death (Abal et al., 2003).”
BackgroundLocalized delivery of immunotherapy via implantable scaffolds for breast cancer treatment
Hope, A., Wade, S. J., Aghmesheh, M., & Vine, K. L. (2021) · Journal of Controlled Release · doi:10.1016/j.jconrel.2021.11.043 · Cited by 40
The Role of α1-Adrenoceptor Antagonists in the Treatment of Prostate and Other Cancers
Batty, M., Pugh, R., Rathinam, I., Simmonds, J. B., Walker, E., Forbes, A., Anoopkumar‐Dukie, S., McDermott, C., Spencer, B. H., Christie, D., et al. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17081339 · Cited by 41
Zhang, H., & Zhang, H.-L. (2017) · Pharmacognosy Magazine · doi:10.4103/0973-1296.211042 · Cited by 40
Noscapine induces apoptosis in human glioma cells by an apoptosis-inducing factor-dependent pathway
Newcomb, E. W., Lukyanov, Y., Smirnova, I., Schnee, T., & Zagzag, D. (2008) · Anti-Cancer Drugs · doi:10.1097/cad.0b013e3282ffd68d · Cited by 42
Schneider, L. X., Eßmann, F., Kletke, A., et al. (2007) · Oncogene · doi:10.1038/sj.onc.1210628 · Cited by 40
“Nevertheless, resistance and a decreased sensitivity to paclitaxel represent an emerging problem in chemotherapy (Abal et al., 2003).”
Xu, H., Huang, Y., Wu, Y., Zhao, Y., Xiao, W., Lin, Q., Sun, H., Dai, W. H., & Chen, G. (2010) · Cell Cycle · doi:10.4161/cc.9.14.12406 · Cited by 39
“Paclitaxel and related taxanes exhibit potent anticancer activities by promoting tubulin polymerization and microtubule stabilization, which is followed by mitotic arrest and apoptosis.(3,4) These compounds are effective against a wide array of malignancies including refractory ovarian cancer, metastatic breast cancer…”
BackgroundGuo, F., Zhang, H., Jia, Z., Cui, M., & Tian, J. (2018) · Europe PMC (PubMed Central) · Cited by 38
Chen, J., Yan, J., Hu, J., et al. (2015) · RSC Advances · doi:10.1039/c5ra14888j · Cited by 37
A synergistic combination therapy with paclitaxel and doxorubicin loaded micellar nanoparticles
Wang, Y., Ma, S., Xie, Z., & Zhang, H. (2014) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2013.12.051 · Cited by 37
Kurebayashi, J., Yamamoto, Y., Kurosumi, M., Okubo, S., Nomura, T., Tanaka, K., & Sonoo, H. (2006) · PubMed · Cited by 37
Oxaliplatin induces drug resistance more rapidly than cisplatin in H69 small cell lung cancer cells
Stordal, B., Davey, M. W., & Davey, R. (2005) · Cancer Chemotherapy and Pharmacology · doi:10.1007/s00280-005-0148-7 · Cited by 36
“Taxanes bind to and stabilise microtubules and block cell cycle progression through centrosomal impairment, induction of abnormal spindles and suppression of spindle microtubule dynamics [53].”
BackgroundCardiac glycosides inhibit cancer through Na/K-ATPase-dependent cell death induction
Geng, X., Wang, F., Tian, D., Huang, L., Streator, E. S., Zhu, J., Kurihara, H., He, R., Yao, X., Zhang, Y., et al. (2020) · Biochemical Pharmacology · doi:10.1016/j.bcp.2020.114226 · Cited by 36
Marco, J. A., García-Pla, J., Cardá, M., Murga, J., Falomir, E., Trigili, C., Notararigo, S., Díaz, J. F., & Barasoaı́n, I. (2011) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2011.02.011 · Cited by 35
Self-citationArsenite-induced mitotic death involves stress response and is independent of tubulin polymerization
Taylor, B. F., McNeely, S., Miller, H. L., et al. (2008) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2008.02.030 · Cited by 35
“It has been reported that paclitaxel's induction of apoptosis canoccurdue to aberrantmitosis or to enteringamultinucleatedG1-like state subsequent to mitotic slippage, depending on cell type and drug schedule (Abal et al., 2003).”
BackgroundTaxane Refractory Prostate Cancer
Mathew, P. F., & DiPaola, R. S. (2007) · The Journal of Urology · doi:10.1016/j.juro.2007.04.032 · Cited by 35
Han, S. J., Kim, J.-H., Kim, J. I., & Park, K. M. (2016) · Scientific Reports · doi:10.1038/srep27775 · Cited by 33
Myc Prevents Apoptosis and Enhances Endoreduplication Induced by Paclitaxel
Gatti, G., Maresca, G., Natoli, M., Florenzano, F., Nicolin, A., Felsani, A., & D’Agnano, I. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005442 · Cited by 37
“To activate apoptosis in these phases of cell cycle, we used PTX, a drug that induces suppression of spindle microtubule dynamics and inhibits mitosis occurrence [35].”
BackgroundMethodInfluentialSchedule Dependent Efficacy of Gefitinib and Docetaxel for Bladder Cancer
Kassouf, W., Luongo, T., Brown, G. A., et al. (2006) · The Journal of Urology · doi:10.1016/j.juro.2006.03.072 · Cited by 34
Silakit, R., Kittirat, Y., Thongchot, S., Loilome, W., Techasen, A., Ungarreevittaya, P., Khuntikeo, N., Yongvanit, P., Yang, J. H., Kim, N. H., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0199827 · Cited by 34
Rahimi, A., Esmaeili, Y., Dana, N., Dabiri, A., Rahimmanesh, I., Jandaghian, S., Vaseghi, G., Shariati, L., Zarrabi, A., Javanmard, S. H., et al. (2023) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2023.106476 · Cited by 36
Wang, R. C., Chen, X., Parissenti, A. M., Joy, A. A., Tuszyński, J. A., Brindley, D. N., & Wang, Z. (2017) · PLoS ONE · doi:10.1371/journal.pone.0182400 · Cited by 33
Plasma polymerized nanoparticles effectively deliver dual siRNA and drug therapy in vivo
Michael, P. L., Lam, Y. T., Filipe, E. C., Tan, R. P., Chan, A., Lee, B. S. L., Feng, N., Hung, J., Cox, T. R., Santos, M., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-69591-x · Cited by 32
Chesnokov, M. S., Halasi, M., Borhani, S., Arbieva, Z. H., Shah, B. N., Oerlemans, R., Khan, I., Camacho, C. J., & Gartel, A. L. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03978-0 · Cited by 35
Pegylation of Nanoliposomal Paclitaxel Enhances its Efficacy in Breast Cancer
Esfahani, M. K. M., Alavi, S. E., Akbarzadeh, A., Ghassemi, S., Saffari, Z., Zarabi, M. F., & Chiani, M. (2014) · Tropical Journal of Pharmaceutical Research · doi:10.4314/tjpr.v13i8.1 · Cited by 32
“It belongs to taxanes family of anti-tumor activity [7,8].”
BackgroundChen, H., Zhu, X., Sun, R., Ma, P., Zhang, E., Wang, Z., Fan, Y., Zhou, G.-X., & Mao, R. (2020) · Investigational New Drugs · doi:10.1007/s10637-020-00951-0 · Cited by 32
“Cisplatin, oxaliplatin, paclitaxel, docetaxel, leucovorin, oxaliplatin and irinotecan are other commonly used drugs for PDAC therapy [23, 24].”
BackgroundBioactive Molecules of Endophytic Fungi and Their Potential in Anticancer Drug Development
Kumar, S., Aharwal, R. P., Jain, R., et al. (2021) · Current Pharmacology Reports · doi:10.1007/s40495-021-00251-y · Cited by 32
Huang, P., Li, F., Mo, Z., Geng, C., Wen, F., Zhang, C., Guo, J., Wu, S., Li, L., Brünner, N., et al. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.669270 · Cited by 31
Demeule, M., Charfi, C., Currie, J.-C., Zgheib, A., Danalache, B. A., Béliveau, R., Marsolais, C., & Annabi, B. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14091910 · Cited by 33
Paclitaxel targets VEGF-mediated angiogenesis in ovarian cancer treatment.
Ai, B., Bie, Z., Zhang, S., et al. (2016) · PubMed · Cited by 31
Stefański, T., Mikstacka, R., Kurczab, R., Dutkiewicz, Z., Kucińska, M., Murias, M., Zielińska‐Przyjemska, M., Cichocki, M., Teubert, A., Kaczmarek, M., et al. (2017) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2017.11.050 · Cited by 32
Nano-Based Drug Delivery and Targeting to Overcome Drug Resistance of Ovarian Cancers
McFadden, M., Singh, S. K., Oprea‐Ilies, G., & Singh, R. (2021) · Cancers · doi:10.3390/cancers13215480 · Cited by 32
Forster, M. D., Kaye, S. B., Oza, A. M., et al. (2007) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-06-1653 · Cited by 31
“The taxanes paclitaxel and docetaxel inhibit cell proliferation by stabilizing microtubule dynamics, thereby inducing aberrant spindle formation during mitosis, mitotic cell-cycle arrest, and apoptotic cell death (1).”
BackgroundVilanova, C., Torijano‐Gutiérrez, S., Díaz‐Oltra, S., et al. (2014) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2014.09.053 · Cited by 31
Blagosklonny, M. V., Demidenko, Z. N., Giovino, M. A., et al. (2006) · Cell Cycle · doi:10.4161/cc.5.14.3113 · Cited by 31
Prell, R. A., Gearin, L., Simmons, A. D., VanRoey, M. J., & Jooss, K. U. (2006) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-005-0116-4 · Cited by 31
“Its primary mechanism of action is via increasing tubulin polymerization and microtubule assembly and inhibiting tubulin depolymerization, resulting in cell cycle arrest at the G2/M interface [6–9].”
BackgroundcircRNAs in drug resistance of breast cancer
Mısır, S., Yaman, S. Ö., Petrović, N., Sümer, C., Hepokur, C., & Aliyazıcıoğlu, Y. (2022) · Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics · doi:10.32604/or.2022.027547 · Cited by 31
Chang, C.-C., Liang, Y., Klutz, A. M., et al. (2006) · Cancer Chemotherapy and Pharmacology · doi:10.1007/s00280-006-0214-9 · Cited by 30
“Paclitaxel, a taxane, interferes with the depolymerization of microtubules, causing cell cycle arrest in mitosis and subsequent induction of apoptosis [3].”
BackgroundYole, M., Wickstrom, M. L., & Blakley, B. R. (2006) · Toxicology · doi:10.1016/j.tox.2006.11.062 · Cited by 30
Multimodality Imaging Review of HER2-positive Breast Cancer and Response to Neoadjuvant Chemotherapy
Portnow, L. H., Kochkodan-Self, J., Maduram, A., et al. (2023) · Radiographics · doi:10.1148/rg.220103 · Cited by 29
Hage‐Sleiman, R., Herveau, S., Matera, E., Laurier, J.-F., & Dumontet, C. (2010) · BMC Cancer · doi:10.1186/1471-2407-10-135 · Cited by 28
“lateral polymerization and suppresses microtubule dynamics [ 45 ].”
BackgroundSkobeleva, N., Menon, S., Weber, L., et al. (2007) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-06-0602 · Cited by 29
“Induction of cell death by microtubule-targeting agents is most potent when treated cells are in mitosis (32, 33).”
BackgroundThe Role of p27 Kip1 in Dasatinib-Enhanced Paclitaxel Cytotoxicity in Human Ovarian Cancer Cells
Le, X., Mao, W., He, G., Claret, F.-X., Xia, W., Ahmed, A. A., Hung, M., Siddik, Z. H., & Bast, R. C. (2011) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djr280 · Cited by 28
“Mitotic slippage is well known to induce a multinucleated phenotype (54,55) and postmitotic cell death (54,56,57).”
Current Research and Development of Chemotherapeutic Agents for Melanoma
Hsan, K. M., Chen, C., & Shyur, L. (2010) · Cancers · doi:10.3390/cancers2020397 · Cited by 27
“These compounds can bind with tubulin and thus prevent the formation of microtubules [29].”
BackgroundYong, K. J., Milenic, D. E., Baidoo, K. E., et al. (2013) · British Journal of Cancer · doi:10.1038/bjc.2013.189 · Cited by 28
“The resultant mitotic arrest triggers rapid onset of the p53-independent apoptotic pathway (Abal et al, 2003).”
BackgroundTagliamento, M., Genova, C., Rossi, G., Coco, S., Rijavec, E., Bello, M. G. D., Boccardo, S., Grossi, F., & Alama, A. (2019) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2019.1627326 · Cited by 29
“to anaphase, resulting in mitotic arrest and subsequent apoptosis [11,12].”
BackgroundTargeting the Microtubular Network as a New Antimyeloma Strategy
Feng, R., Li, S., Lu, C., et al. (2011) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-11-0234 · Cited by 28
“The coordinatedprocesses of cell-cycle progression, cell growth, and apoptosis are dysfunctional in cancer (1, 2).”
BackgroundDan, K., Shlofmitz, E., Khalid, N. M., et al. (2019) · American Heart Journal · doi:10.1016/j.ahj.2019.12.012 · Cited by 27
A look into the link between centrosome amplification and breast cancer
Zhang, Y., Tian, J., Qu, C., Peng, Y., Lei, J., Sun, L., Zong, B., & Liu, S. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110924 · Cited by 28
Breaking Tolerance in a Mouse Model of Multiple Myeloma by Chemoimmunotherapy
Sharabi, A., & Haran‐Ghera, N. (2010) · Advances in cancer research · doi:10.1016/s0065-230x(10)07001-6 · Cited by 27
Fluorescent Taxoid Probes for Microtubule Research
Barasoaı́n, I., Díaz, J. F., & Andreu, J. M. (2010) · Methods in cell biology · doi:10.1016/s0091-679x(10)95019-x · Cited by 27
Self-citationChoe, M. S., Chen, Z., Klass, C. M., et al. (2007) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-06-2959 · Cited by 27
Adjuvant effect of docetaxel on the immune responses to influenza A H1N1 vaccine in mice
Chen, J., Yuan, L., Fan, Q., et al. (2012) · BMC Immunology · doi:10.1186/1471-2172-13-36 · Cited by 26
“At the late 1970s, paclitaxel was discovered able to blocks mitosis and cause the death of cancer cells by binding to and stabilizing microtubules [16,17].”
BackgroundHazane‐Puch, F., Arnaud, J., Trocmé, C., Faure, P., Laporte, F., & Champelovier, P. (2016) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1871520615666150819095426 · Cited by 26
Loss of EGFR induced autophagy sensitizes hormone refractory prostate cancer cells to adriamycin
Xu, S., & Weihua, Z. (2011) · The Prostate · doi:10.1002/pros.21337 · Cited by 26
Balcer‐Kubiczek, E. K., Attarpour, M., Jiang, J., Kennedy, A. S., & Suntharalingam, M. (2006) · Chemotherapy · doi:10.1159/000094869 · Cited by 26
Jha, S. K., Singh, N., Shanker, O. R., Antil, I., Baghel, J. S., Huddar, V. G., & Tripathi, R. (2025) · Frontiers in Natural Products · doi:10.3389/fntpr.2025.1635197 · Cited by 29
Yu, Y., Fu, X., Ran, Q., Yang, K., Wen, Y., Li, H., & Wang, F. (2017) · Biochimie · doi:10.1016/j.biochi.2017.09.005 · Cited by 25
RetractedLegrier, M.-E., Oudard, S. M., Judde, J.-G., Guyader, C., Pinieux, G. D. B. D., Boyé, K., de Crémoux, P., Dutrillaux, B., & Poupon, M. F. (2007) · British Journal of Cancer · doi:10.1038/sj.bjc.6603553 · Cited by 25
“Taxanes block tubulin depolymerisation, resulting in impairment of cellular mitosis (Horwitz, 1994), generating nuclear abnormalities and multipolar divisions, ultimately leading to cell death (Abal et al, 2003).”
BackgroundSites of biosynthesis and storage of Taxol in Taxus media (Rehder) plants: Mechanism of accumulation
Soliman, S. S. M., & Raizada, M. N. (2020) · Phytochemistry · doi:10.1016/j.phytochem.2020.112369 · Cited by 24
Therapeutic Potential of PARP Inhibitors in the Treatment of Gastrointestinal Cancers
Alhusaini, A., Cannon, A., Maher, S. G., Reynolds, J. V., & Lynam-Lennon, N. (2021) · Biomedicines · doi:10.3390/biomedicines9081024 · Cited by 24
“The primary mechanism of anti-microtubule agents is to halt tumour cell mitosis by disrupting microtubule function [147,148].”
BackgroundSynthesis and biological evaluation of novel anticancer bivalent colchicine–tubulizine hybrids
Malysheva, Y. B., Combes, S., Allegro, D., et al. (2012) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2012.05.072 · Cited by 24
Decrease in c-Myc activity enhances cancer cell sensitivity to vinblastine
Bressin, C. L., Bourgarel‐Rey, V., Carr??, M., Pourroy, B., Arango, D., Braguer, D., & Barra, Y. (2006) · Anti-Cancer Drugs · doi:10.1097/00001813-200602000-00009 · Cited by 24
Dittmann, H., Jusufoska, A., Dohmen, B. M., Smyczek-Gargya, B., Fersis, N., Pritzkow, M., Kehlbach, R., Vonthein, R., Machulla, H.-J., & Bares, R. (2009) · Nuclear Medicine and Biology · doi:10.1016/j.nucmedbio.2008.10.012 · Cited by 24
Paclitaxel/Luteolin Coloaded Dual‐Functional Liposomes for Esophageal Cancer Therapy
Sun, C., Xie, F., Zhang, H., Feng, L., Wang, Y., Huang, C., Cui, Z., Luo, C., Zhang, L., & Wang, Q. (2025) · Advanced Science · doi:10.1002/advs.202411930 · Cited by 25
Complications from pharmacotherapy
Nabors, B., Surboeck, B., & Grisold, W. (2016) · Handbook of clinical neurology · doi:10.1016/b978-0-12-802997-8.00014-1 · Cited by 23
MicroRNAs: key players of taxane resistance and their therapeutic potential in human cancers
Cui, S., Wang, R., & Chen, L. (2013) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12131 · Cited by 25
“They both inhibit the process of cell division, causing a ‘frozen mitosis’ by stabilizing microtubules and thus preventing disassembly [7].”
BackgroundDrug-Eluting Stent - Importance of Clinico-Pathological Correlations -
Hao, H., Ishibashi‐Ueda, H., Tsujimoto, M., et al. (2011) · Circulation Journal · doi:10.1253/circj.cj-11-0393 · Cited by 22
Barrón-Gallardo, C. A., García‐Chagollán, M., Morán-Mendoza, A. J., Delgadillo-Cristerna, R., Martínez-Silva, M. G., Villaseñor-Garcı́a, M. M., Aguilar‐Lemarroy, A., & Jave‐Suárez, L. F. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.991706 · Cited by 22
“The treatment of HER2+ breast cancer includes the administration of chemotherapy and trastuzumab, a monoclonal antibody against the HER2 receptor (Abal et al., 2003; Harbeck and Gnant, 2017; Waks and Winer, 2019).”
BackgroundQi, Y., Ding, Z., Yao, Y., et al. (2018) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2018.7138 · Cited by 22
RetractedStauffer, S., Zeng, Y., Santos, M., Zhou, J., Chen, Y., & Dong, J. (2019) · Journal of Cell Science · doi:10.1242/jcs.236000 · Cited by 25
“, 2011) or through aberrant mitosis and eventual death in G1 (Abal et al., 2003).”
BackgroundHou, D., Huibregtse, B. A., Eppihimer, M. J., et al. (2016) · EuroIntervention · doi:10.4244/eijv12i6a128 · Cited by 22
Targeting synuclein-γ to counteract drug resistance in cancer
Singh, V. K., & Jia, Z. (2007) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.12.1.59 · Cited by 21
“These microtubule-disrupting agents are thought to arrest cells in mitosis by triggering spindle assembly checkpoint activation, this results in the cells being arrested in the mitotic phase without entering anaphase ( Figure 2 ) [60-62] .”
BackgroundMohapatra, S., Saha, A., Mondal, P., Jana, B., Ghosh, S., Biswas, A., & Ghosh, S. (2016) · Advanced Healthcare Materials · doi:10.1002/adhm.201600718 · Cited by 20
Impact of Docetaxel on blood-brain barrier function and formation of breast cancer brain metastases
Bernatz, S., Ilina, E. I., Devraj, K., Harter, P. N., Mueller, K. M., Kleber, S., Braun, Y., Penski, C., Renner, C., Halder, R., et al. (2019) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-019-1427-1 · Cited by 19
“Furthermore, taxanes induce apoptosis, however the underlying mechanisms are not yet fully understood [18, 19].”
BackgroundA Review of Treatment-Induced Pulmonary Toxicity in Breast Cancer
Mo, H., Jazieh, K., Brinzevich, D., & Abraham, J. (2021) · Clinical Breast Cancer · doi:10.1016/j.clbc.2021.05.014 · Cited by 21
Hess-Wilson, J. K., Daly, H. K., Zagórski, W., Montville, C. P., & Knudsen, K. E. (2006) · Cancer Research · doi:10.1158/0008-5472.can-06-2249 · Cited by 21
“It has been hypothesized that the ability of paclitaxel to interfere with cytokinesis would make dividing cells more sensitive; however, there has been significant variation in cellular sensitivity to paclitaxel (46).”
BackgroundChemotherapy-Induced Alopecia by Docetaxel: Prevalence, Treatment and Prevention
Perez, A. M., Haberland, N. I., Miteva, M. I., et al. (2024) · Current Oncology · doi:10.3390/curroncol31090423 · Cited by 20
“Because taxanes initiate tumor cell death by directly interfering with the cell cycle, the ability to arrest the HF cell cycle makes the HFs less susceptible to taxane-induced damage in CIA [35,66,75–80].”
BackgroundBattaglia, A. M., Sacco, A., Giorgio, E., Petriaggi, L., Elzanowska, J., Cruz, A. R., Rocha, L., Pereira, C. E., Moraes, M. C. S., Palazzo, L., et al. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1532097 · Cited by 21
Novel application of drug-coated balloons in coronary heart disease: A narrative review
Wang, L., Li, X., Li, T. X., et al. (2023) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2023.1055274 · Cited by 20
Paños, J., Díaz‐Oltra, S., Sánchez‐Peris, M., García-Pla, J., Murga, J., Falomir, E., Cardá, M., Redondo‐Horcajo, M., Díaz, J. F., Barasoaı́n, I., et al. (2013) · Organic & Biomolecular Chemistry · doi:10.1039/c3ob40854j · Cited by 20
Self-citationZhu, D., Zha, X., Hu, M., Tao, A.-D., Zhou, H., Zhou, X., & Sun, Y. (2012) · Medical Oncology · doi:10.1007/s12032-012-0239-3 · Cited by 20
“Paclitaxel can bind tubulin to promote tubulin polymerization and block depolymerization of microtubules, thereby disrupting dynamic balance of tubulin polymerization/depolymerization and spindle function, inhibiting mitosis to block cells in G2/M phase, ultimately leading to apoptosis [10, 11].”
BackgroundRoles of BCL-2 and MDR1 expression in the efficacy of paclitaxel-based lung cancer chemoradiation.
Maráz, A., Furák, J., Pálföldi, R., et al. (2011) · PubMed · Cited by 20
Demidenko, Z. N., Halicka, D. H., Kunicki, J., McCubrey, J. A., Darżynkiewicz, Z., & Blagosklonny, M. V. (2005) · Cancer Research · doi:10.1158/0008-5472.can-04-4428 · Cited by 20
Ferroptosis: a novel strategy to overcome chemoresistance in gynecological malignancies
Xu, J., Zheng, B., Wang, W., & Zhou, S. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1417750 · Cited by 26
Taxanes in the Treatment of Advanced Gastric Cancer
Kang, B., Kwon, O., Chung, H. Y., Yu, W., & Kim, J. G. (2016) · Molecules · doi:10.3390/molecules21050651 · Cited by 19
“As their name suggests, taxanes were first derived from natural sources, yet now are synthesized artificially (Table 1) [16].”
BackgroundAng, E. S. M., Pavlos, N. J., Chim, S. M., Feng, H., Scaife, R. M., Steer, J. H., Zheng, M., & Xu, J. (2011) · Journal of Cellular Biochemistry · doi:10.1002/jcb.23423 · Cited by 19
“Bars, 20mm. 952 EFFECTS OF PACLITAXEL ON OSTEOCLASTS JOURNAL OF CELLULAR BIOCHEMISTRY Previous studies have shown that paclitaxel binds to b-tubulin and inhibits microtubule dynamic instability, leading to apoptosis in several cell types [Abal et al., 2003; Bhalla, 2003].”
BackgroundInfluentialCell cycle‐tailored targeting of metastatic melanoma: Challenges and opportunities
Haass, N. K., & Gabrielli, B. G. (2017) · Experimental Dermatology · doi:10.1111/exd.13303 · Cited by 20
Björkman, P., Auvinen, T., Hakovirta, H. H., et al. (2018) · Annals of Vascular Surgery · doi:10.1016/j.avsg.2018.04.014 · Cited by 19
Less Is More: Developments in Nanotechnology for Antirestenosis Therapies
Trepanier, C. M., Burke‐Kleinman, J., Strauss, B. H., Santerre, J. P., & Bendeck, M. P. (2023) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.123.318450 · Cited by 19
Overexpression of centrosomal protein Nlp confers breast carcinoma resistance to paclitaxel
Zhao, W., Song, Y., Xu, B., et al. (2012) · Cancer Biology & Therapy · doi:10.4161/cbt.13.3.18697 · Cited by 18
“Paclitaxel blocks cells in the G2-M phase of the cell cycle and such cells are unable to form a normal mitotic apparatus and then undergo apoptosis.(39,40) Figure 3.”
BackgroundBailey, S. R. (2009) · Journal of Interventional Cardiology · doi:10.1111/j.1540-8183.2009.00449.x · Cited by 18
Metadata
- Authors
- Abal, M., Andreu, J., & Barasoain, I.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- ORCID
- Venue
- Current Cancer Drug Targets
- Publisher
- Bentham Science Publishers Ltd.
- Published
- 2003-06-01
- Volume
- 3
- Issue
- 3
- Pages
- 193-203
- ISSN
- 1568-0096 (ISSN-L)
- OpenAlex
- W2164778107
- Cited by
- 383
- References
- 0
- Citations by year
- 2026: 7 · 2025: 14 · 2024: 18 · 2023: 21 · 2022: 22 · 2021: 22 · 2020: 14 · 2019: 19 · 2018: 22 · 2017: 21 · 2016: 23 · 2015: 11 · 2014: 22 · 2013: 14 · 2012: 16
- FWCI
- 5.35
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Current Cancer Drug Targets (publishedVersion)
- PubMed (publishedVersion)
- DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion)
- Funders
- Fundación Científica Asociación Española Contra el Cáncer
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Health Sciences › Medicine › Oncology › Cancer Treatment and Pharmacology
- Physical Sciences › Chemistry › Organic Chemistry › Heterocyclic Compound Synthesis and Bioactivity
- Keywords
- taxanes, paclitaxel, microtubules, centrosome, spindle microtubules, mitosis, mitotic slippage, apoptosis, Bcl-2 phosphorylation, p53, taxane resistance, cell cycle checkpoints, antimitotic agents
- MeSH terms
- Animals, Cell Cycle, Humans, Microtubules, Drug Delivery Systems, Paclitaxel, Centrosome
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