Sunitinib, sorafenib and mTOR inhibitors in renal cancer

Sinisa Radulovic1, Snezana K Bjelogrlic

  • 1Department of Translational Research, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia. sinisar@ncrc.ac.yu

Insights

Targeted therapies like sorafenib, sunitinib, and temsirolimus offer new hope for advanced renal cell carcinoma (RCC) by inhibiting key pathways. Understanding VHL gene mutations and targeted agent mechanisms is crucial for optimizing treatment and overcoming resistance.

Area of Science:

  • Oncology
  • Molecular Biology
  • Pharmacology

Background:

  • Renal cell carcinoma (RCC) tumorigenesis is linked to von Hippel-Lindau (VHL) gene mutations, leading to increased proangiogenic factors and vascular tumors.
  • Mammalian target of rapamycin (mTOR) pathway activation, driven by hypoxia-inducible factor (HIF), promotes cell proliferation in RCC.

Purpose of the Study:

  • To review the development and current guidelines for targeted agents in advanced RCC treatment.
  • To explore future directions in optimizing targeted therapy, including combinations, sequential use, and resistance mechanisms.

Main Methods:

  • Review of clinical studies and FDA-approved targeted agents for advanced RCC.
  • Analysis of mechanisms of action for sorafenib, sunitinib, and temsirolimus.
  • Examination of current treatment guidelines based on patient risk stratification.

Main Results:

  • Three targeted agents approved: sorafenib and sunitinib (VEGFR/PDGFR inhibitors) and temsirolimus (mTOR inhibitor).
  • Established guidelines recommend sunitinib as first-line for good/intermediate-risk, temsirolimus for poor-risk, and sorafenib as second-line therapy.
  • Targeted therapies have significantly advanced advanced RCC treatment.

Conclusions:

  • Targeted therapies targeting angiogenesis and mTOR pathways represent a significant advancement in treating advanced RCC.
  • Future research should focus on optimizing drug combinations, sequential use, understanding resistance, and identifying biomarkers for personalized treatment.

Related Concept Videos

mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against specific...
Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a rapamycin-insensitive companion...
Combination Therapies and Personalized Medicine02:50

Combination Therapies and Personalized Medicine

Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
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...