Related Experiment Video
Updated: May 11, 2026

Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
Targeted therapy with kinase inhibitors in aggressive endocrine tumors
Vincenzo Marotta1, Maria Domenica Franzese, Michela Del Prete
1Federico II University, Department of Clinical Medicine and Surgery, Italy. vinc.endo@libero.it
Introduction:
Kinase inhibitors (KIs) are a class of anticancer drugs that inhibit activity of the enzymes protein kinases, which regulate crucial cellular processes and have a demonstrated role in human oncogenesis. Treatment of advanced forms of endocrine cancer which are not responsive to cytotoxic chemotherapies is challenging and use of KIs is gaining a growing role in this field.
Areas Covered:
The authors summarize the main genetic alterations known to be linked to endocrine tumors, indicating the rationale for utilizing KIs. Furthermore, they present an updated analysis of clinical trials available on PubMed Central, which were pertinent to the activities of KIs in aggressive endocrine cancer. The authors also discuss the adverse effects of KIs and summarize likely involved underlying mechanisms.
Expert Opinion:
KIs are effective in obtaining a radiological disease control and an improvement of progression-free survival in several forms of endocrine cancer but will never deliver a knockout blow of the disease, due to mechanisms of adaptation to circumvent the specific molecular blockade. The new frontier of KIs treatment is to identify agents that could synergize activity of KIs. The true goal will be to perform an overall genotyping of each tumor, thus predicting the impact of combined targeted therapies in the context of a particular constellation of mutant genes.
Insights
Kinase inhibitors (KIs) show promise in controlling advanced endocrine cancers, improving progression-free survival. However, they do not cure the disease, necessitating research into synergistic therapies and tumor genotyping for combined treatments.
Area of Science:
- Oncology
- Pharmacology
- Genetics
Background:
- Kinase inhibitors (KIs) target protein kinases, crucial in cell processes and oncogenesis.
- KIs are increasingly used for advanced endocrine cancers resistant to chemotherapy.
Purpose of the Study:
- To review genetic alterations in endocrine tumors and the rationale for KI use.
- To analyze clinical trials on KIs in aggressive endocrine cancer.
- To discuss KI adverse effects and their mechanisms.
Main Methods:
- Literature review of PubMed Central clinical trials.
- Summary of genetic alterations in endocrine tumors.
- Analysis of KI efficacy, adverse effects, and resistance mechanisms.
Main Results:
- KIs achieve radiological disease control and improve progression-free survival in endocrine cancers.
- Mechanisms of adaptation can circumvent KI molecular blockade, preventing a cure.
- Identifying synergistic agents and comprehensive tumor genotyping are key for future treatments.
Conclusions:
- KIs offer significant benefits but not a cure for endocrine cancers.
- Future strategies involve combining KIs with other agents to overcome resistance.
- Personalized medicine through tumor genotyping will guide combined targeted therapies.
More Related Videos
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Combination Therapies and Personalized Medicine
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
Transducer Mechanism: Enzyme-Linked Receptors
Major types that are helpful drug targets include:
Mitogens and the Cell Cycle
M-Cdk Drives Transition Into Mitosis
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...

