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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.
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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]
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Aguilar‐Santelises, M., Mozart, M., Scuderi, R., et al. (2006) · Nitric Oxide · doi:10.1016/j.niox.2006.03.007 · Cited by 3
Langner, C., & Ott, A. (2007) · Histopathology · doi:10.1111/j.1365-2559.2007.02672.x · Cited by 3
“Both drugs bind to the b-subunit of tubulin and the principal antitumour activity has been ascribed to the promotion of microtubule assembly and stabilization of the polymers against depolymerization, thus causing centrosomal impairment, ultimately leading to cell-cycle arrest.(5) In addition, the disruption of microt…”
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Fitzgerald, P. J., & Otake, H. (2008) · Revista Española de Cardiología (English Edition) · doi:10.1016/s1885-5857(09)60001-3 · Cited by 3
“Paclitaxel is a cytotoxic drug, which suppresses smooth muscle cell and endothelial cell proliferation by disrupting microtubule dynamic cells in the mitosis phase of the cell cycle.(35) Although results of MR Taxus stents demonstrated a moderate inflammatory response without evidence of increased amounts of fibrin de…”
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Wang, R., Wang, H. H., & Wang, Z. (2017) · Journal of Visualized Experiments · doi:10.3791/55027 · Cited by 2
Helena, J., Joubert, A. M., Mabeta, P., et al. (2021) · Cells · doi:10.3390/cells10082105 · Cited by 3
Taxus spp.: Botany, Horticulture, and Source of Anti‐Cancer Compounds
DeLong, J. M., & Prange, R. K. (2006) · Horticultural reviews · doi:10.1002/9780470767986.ch6 · Cited by 3
Auvray, M., Koenen, T., Dybkov, O., Urlaub, H., & Lukinavičius, G. (2025) · Nature Communications · doi:10.1038/s41467-025-67319-x · Cited by 2
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Shi, L., Yu, L., Zhong, D., et al. (2018) · AIDS · doi:10.1097/qad.0000000000001808 · Cited by 2
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Ide, K., Kawano, T., Shirakawa, J., et al. (2023) · Oncology Reports · doi:10.3892/or.2023.8619 · Cited by 2
Ramasamy, K. (2023) · Bioinformation · doi:10.6026/97320630019754 · Cited by 2
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Dustin, S. M., Jeffus, S. K., & Stelow, E. B. (2014) · Diagnostic Cytopathology · doi:10.1002/dc.23046 · Cited by 2
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Khan, A. K., Jain, A. G., Afridi, S., Wazir, M., Rao, J. S., & Ahmad, S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-819457-7.00006-2 · Cited by 2
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Kingston, D. G. I. (2010) · Springer eBooks · doi:10.1007/978-90-481-9704-0_1 · Cited by 2
Thomas, L. J., Steinberg, R. L., Packiam, V. T., et al. (2022) · Clinical Genitourinary Cancer · doi:10.1016/j.clgc.2022.09.004 · Cited by 1
Schirizzi, A., Renna, N., Leonardis, G. D., Montanaro, R., Mastropasqua, F., Graziano, G., Riganti, C., Pisano, I., Laghezza, A., Abate, C., et al. (2025) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-025-03476-7 · Cited by 1
“One of these models was resistant to the cytotoxic action of the chemotherapeutic agent PTX, a taxane known as antimitotic drug that blocks the disassembly of interphase microtubules, leading to cell cycle arrest [33–35].”
Gu, Y., Gai, C., Zou, S., et al. (2025) · Molecules · doi:10.3390/molecules30234538 · Cited by 1
“Microtubule-targeting agents (MTAs) interfere with microtubule dynamics by inhibiting either polymerization or depolymerization, thereby blocking mitosis in cancer cells and inducing G 2 /M phase arrest and apoptosis [9–11].”
Lopez-Aguileta, L., Martín‐Encinas, E., Knudsen, B. R., Tesauro, C., Schirizzi, A., Montanaro, R., D’Alessandro, R., Perrone, M. G., Stefanachi, A., Contino, M., et al. (2026) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2026.118782 · Cited by 1
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Andrés, V., Fuster, J. J., Silvestre-Roig, C., & Wessely, R. (2012) · Humana Press eBooks · doi:10.1007/978-1-61779-906-8_8 · Cited by 1
Niu, Y., Zhang, T., Wang, Y., et al. (2008) · Chinese Journal of Clinical Oncology · doi:10.1007/s11805-008-0016-4 · Cited by 1
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Doshi, M., Shah, D., & Sojitra, P. N. (2019) · Springer eBooks · doi:10.1007/978-3-319-92600-1_7 · Cited by 1
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Quitmann, C. M., Rust, S., Reunert, J., et al. (2021) · Child Neurology Open · doi:10.1177/2329048x211034969 · Cited by 1
Natural products in chemotherapy of cancers
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Younger, N. S., & Borno, H. T. (2022) · International Journal of Cancer Care and Delivery · doi:10.53876/001c.36780 · Cited by 1
Chemotherapeutic Protocols for the Treatment of Breast Cancer
Cavalcanti, I. D. L. (2022) · Springer eBooks · doi:10.1007/978-3-031-10839-6_4 · Cited by 1
Shamloul, G., Desai, M., & Laslett, N. (2023) · Cureus · doi:10.7759/cureus.37590 · Cited by 1
“Docetaxel (Taxotere) is a taxane chemotherapeutic agent that works by disrupting microtubule function and thus blocking cell cycle progression [7].”
BackgroundJamil, K., Subhani, S., & Atilli, S. S. (2015) · Acta Medica International · doi:10.5530/ami.2015.2.6 · Cited by 1
Wang, Y., Gu, Q., Yan, K., et al. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.08.002 · Cited by 1
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THE EFFECT OF COBALT CHLORIDE PRECONDITIONING ON PACLITAXEL-INDUCED PERIPHERAL NEUROPATHY.
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O’Sullivan, D. (2012) · Open Access Victoria University of Wellington | Te Herenga Waka (Figshare) · doi:10.26686/wgtn.16997467 · Cited by 1
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Luján, M., & Milagros, M. (2012)
Hofmann, P. (2014) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-13615
Evaluation of the Selective Anti-Cancer Activity of Natural and Synthetic Alkaloids
Griffin, C. (2011) · Scholarship at UWindsor (University of Windsor)
Recent Data with Gemcitabine-Based Chemotherapy Combinations in Metastatic Breast Cancer
DeGrendele, H. C., & O'Shaughnessy, J. A. (2003) · Clinical Breast Cancer · doi:10.1016/s1526-8209(11)70448-7
Cortez, B. A. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.41.2014.tde-15122014-143541
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Dijkhuis, A. (2006) · University of Groningen research database (University of Groningen / Centre for Information Technology)
Direktor, Ä., & Wallwiener, D. R. (2008)
Ekinci, A. P., Erdem, Y., & Baykal, C. (2014) · TURKDERM · doi:10.4274/turkderm.48.s26
(2010) · CRC Press eBooks · doi:10.1201/ebk1420073492-c2
Zhao, Y. (2016) · Lu Zone Ul (Laurentian University)
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Seneci, P. (2018) · Elsevier eBooks · doi:10.1016/b978-0-08-099420-8.00001-8
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von Döbeln, G. A. (2018)
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Magnano, S. (2021) · Arrow@dit (Dublin Institute of Technology)
Tang, J. Z., & Rhodes, N. P. (2016) · CRC Press eBooks · doi:10.1201/b10871-11
Schneider, L. (2008) · Univ. Duesseldorf: Duesseldorfer Dokumenten- und Publikationsserver
Richard, S. D., & Buchanan, T. (2018) · Cambridge University Press eBooks · doi:10.1017/9781108178594.028
Rosenthal, D. I., Fuller, C. D., Machtay, M. X., et al. (2006) · Journal of Thoracic Oncology · doi:10.1016/s1556-0864(15)31511-2
Combined Therapy for the Treatment of Cancer
Cavalcanti, I. D. L. (2022) · Springer eBooks · doi:10.1007/978-3-031-10839-6_2
Srdanovic, I., Yang, N., & Ray, S. D. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-824315-2.00216-5
Chen, Y., Yu, J., Wang, Z., et al. (2022) · Diseases & Research · doi:10.54457/dr.202202005
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Feng, R., Li, S., Lu, C., et al. (2023) · doi:10.1158/1535-7163.c.6535426
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Jan, F., Chaudhary, B., Chawla, A., Ovais, S., Mushtaq, S., & Wali, A. F. (2023) · Elsevier eBooks · doi:10.1016/b978-0-443-19094-0.00009-6
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Maritza Garrido, P., & Carmen Romero, O. (2023) · Revista Hospital Clínico Universidad de Chile · doi:10.5354/2735-7996.2023.72916
“Ambos son fármacos que inhiben la replicación celular, induciendo la muerte de las células en proceso proliferativo (9,10) .”
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Liao, J., Song, Q., Li, J., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16575876
Downregulation of PIF1 induce DNA damage and inhibit ovarian cancer cell proliferation via RAD51Preprint
Zhou, Q., Hua, Y.-X., Sun, Q.-Q., Zou, S.-P., Guo, J., Ni, M.-Z., Zhang, S., Liu, S., Guo, Y.-J., Ao, L., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-4495865/v1
Ha, Y. S., Kim, J. W., Lee, J. Y., et al. (2024) · Japanese Journal of Clinical Oncology · doi:10.1093/jjco/hyae099
Warren, B. E., Tan, K., Rajan, D. K., et al. (2024) · JVS Vascular Science · doi:10.1016/j.jvssci.2024.100277
Zhang, J., Zhou, X., & Sun, R. (2025) · Theoretical and Natural Science · doi:10.54254/2753-8818/2024.19989
An Unexpected Cutaneous Response to a Skin Test to Paclitaxel: A Case Report
Gonzalez-Bravo, L., Barbarroja-Escudero, J., Sánchez-González, M. J., et al. (2025) · Clinical Cancer Drugs · doi:10.2174/012212697x367069250707103625
Gu, Y., Gai, C., Wang, J., et al. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5417555
The Role of Runx2 in Microtubule Dynamics and Its Effects on Osteoblast Migration
Winogradzki, M., Patel, S., Holmes, W., Vistal, A., Othman, A. H., & Pratap, J. (2025) · Cytoskeleton · doi:10.1002/cm.70064
Liao, J., Song, Q., Li, J., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16575870
A genetically encoded microtubule bundler for causal dissection of microtubule bundling in cellsPreprint
Watari, S., Chinen, T., Kunitatsu, Y., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.22.700042
“Pharmacological approaches have provided powerful tools to perturb MT polymerization and depolymerization and have been instrumental in elucidating MT-dependent processes such as spindle checkpoint signaling and organelle positioning 19–22 .”
Mansouri, A., Hart, O., Aslanabadi, S., Hartupee, C. D., Yalcin, D., Sinha, G., Chabu, C. Y., Cios, A., Cheng, Z., Ammanamanchi, S., et al. (2026) · Cells · doi:10.3390/cells15060531
“Nab-paclitaxel, a component of GEMPAC, is known to stabilize microtubules and therefore block cell cycle progression and mitotic cytokinesis, inducing apoptosis [57].”
Yim, K. H., Vergara, M., Lee, J., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.10.724123
“Together, these agents act synergistically to induce cytotoxicity and mitotic errors in bladder cancer cells[6, 7].”
Susmitha, A., Galla, R., Eri, G. K., et al. (2026) · Critical Reviews in Analytical Chemistry · doi:10.1080/10408347.2026.2718350
Mechanically Powered Piezoelectric Pulsed‐Field System for Tumor Ablation
Hu, J., You, L., Yu, H., et al. (2026) · Advanced Functional Materials · doi:10.1002/adfm.78088
“…taxane-based chemotherapy is administered systemically and exerts anti-tumor activity by stabilizing microtubules and disrupting mitosis; however, this mechanism primarily affects actively proliferating cells and lacks tumor selectivity [ 55 ], contributing to dose-related systemic toxicities.”
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
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