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Related Concept Videos

Drugs that Stabilize Microtubules01:15

Drugs that Stabilize Microtubules

Microtubules are dynamic structures that undergo cycles of catastrophe and rescue. The microtubules play a central role in cell division by forming the spindle apparatus for segregating the chromosomes. This makes them ideal targets for regulating dividing cells in tumors and malignant cancer cells. Microtubule stabilizing drugs help stabilize the microtubule formation and promote its polymerization. Paclitaxel was the first microtubule stabilizing agent used as anticancer drug in chemotherapy...
Anthelminthic Agents01:15

Anthelminthic Agents

Anthelmintic drugs differ significantly from antiparasitic therapies targeting protozoa, primarily due to differences in parasite biology. Whereas most protozoal treatments act on proliferating cells, anthelmintics are typically directed against mature, nonproliferative helminths. The therapeutic approach considers the helminth's reliance on neuromuscular coordination, glucose metabolism, and microtubular integrity for survival, reproduction, and localization within the host. Most anthelmintics...
Directly Acting Muscle Relaxants: Dantrolene and Botulinum Toxin01:26

Directly Acting Muscle Relaxants: Dantrolene and Botulinum Toxin

Directly acting muscle relaxants like dantrolene and botulinum toxin (BoNT) have distinct mechanisms and applications. Dantrolene, a hydantoin derivative, acts on the ryanodine receptor (RYR1) in skeletal muscle cells. RYR1 are calcium channels present at the sarcoplasmic reticulum membrane. In response to excitation, they release calcium ions from the sarcoplasmic reticulum to the cytosol. Calcium promotes actin-myosin-mediated contraction of muscles.
The binding of dantrolene to the RYR1...
Drugs that Destabilize Microtubules01:10

Drugs that Destabilize Microtubules

Microtubules are dynamic structures and can be regulated by microtubule targeting agents (MTAs). Microtubule destabilizing drugs are a class of MTAs that destabilize and prevent microtubules' polymerization. Both natural and synthetic chemicals can be found under this class of drugs. Vincristine and vinblastine, two vinca alkaloids, and colchicine were among the first to be discovered. These drugs can affect cells in various ways, either by inducing a change in cell morphology, preventing...

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Related Experiment Video

Updated: Jun 18, 2026

Live Imaging to Study Microtubule Dynamic Instability in Taxane-resistant Breast Cancers
06:02

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[What comes after docetaxel?].

C-H Ohlmann1, M Stöckle

  • 1Klinik für Urologie und Kinderurologie, Universitätsklinikum des Saarlandes, Kirrbergerstrasse 1, 66421, Homburg/Saar, Deutschland. Carsten.Ohlmann@uks.eu

Der Urologe. Ausg. A
|November 11, 2009
PubMed
Summary

Docetaxel is standard first-line treatment for castration-resistant prostate cancer (CRPC). For patients progressing after docetaxel, this review explores current options and promising new treatments like abiraterone acetate and MDV3100.

Area of Science:

  • Oncology
  • Urology
  • Medical Chemistry

Background:

  • Docetaxel chemotherapy is the standard first-line treatment for castration-resistant prostate cancer (CRPC).
  • Limited treatment options exist for patients with CRPC who progress after docetaxel therapy.
  • No established treatment has demonstrated a survival benefit in clinical trials for post-docetaxel CRPC.

Purpose of the Study:

  • To review available treatment options for patients with progressive castration-resistant prostate cancer (CRPC).
  • To highlight promising novel therapies currently under clinical investigation for advanced CRPC.
  • To provide an overview of the treatment landscape for CRPC following docetaxel failure.

Main Methods:

  • Literature review of clinical trials and treatment guidelines for CRPC.

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Carotid Artery Infusions for Pharmacokinetic and Pharmacodynamic Analysis of Taxanes in Mice

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Last Updated: Jun 18, 2026

Live Imaging to Study Microtubule Dynamic Instability in Taxane-resistant Breast Cancers
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Generation of Prostate Cancer Cell Models of Resistance to the Anti-mitotic Agent Docetaxel
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Carotid Artery Infusions for Pharmacokinetic and Pharmacodynamic Analysis of Taxanes in Mice
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  • Analysis of data on efficacy and safety of existing and emerging CRPC therapies.
  • Focus on treatments for patients with documented progression after docetaxel.
  • Main Results:

    • Current treatment options for progressive CRPC lack a proven survival benefit.
    • Abiraterone acetate and MDV3100 are promising agents under investigation.
    • Further clinical trials are needed to establish new standards of care.

    Conclusions:

    • The management of docetaxel-refractory CRPC remains a significant clinical challenge.
    • Novel therapeutic agents like abiraterone acetate and MDV3100 show potential for improving outcomes.
    • Ongoing research is crucial for developing effective treatments for advanced prostate cancer.