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Published on: June 18, 2015
Re-Use of Established Drugs for Anti-Metastatic Indications
Frank Entschladen1,2, Dane A Thyssen3, David W Drell4
1MetaVì Labs Inc., 16238 Ranch Road 620 North, Suite F-347, Austin, TX 78717, USA. fentschladen@metavilabs.com.
Abstract:
Most patients that die from cancer do not die due to the primary tumor but due to the development of metastases. However, there is currently still no drug on the market that specifically addresses and inhibits metastasis formation. This lack was, in the past, largely due to the lack of appropriate screening models, but recent developments have established such models and have provided evidence that tumor cell migration works as a surrogate for metastasis formation. Herein we deliver on several examples a rationale for not only testing novel cancer drugs by use of these screening assays, but also reconsider established drugs even of other fields of indication.
Insights
Most cancer deaths result from metastasis, not primary tumors. New screening models allow testing of novel and existing drugs to inhibit cancer cell migration and metastasis formation.
Area of Science:
- Oncology
- Cancer Research
- Drug Discovery
Background:
- Cancer metastasis, the spread of cancer cells from the primary tumor to distant sites, is the primary cause of cancer-related mortality.
- Current therapeutic strategies primarily focus on treating the primary tumor, with limited options available to specifically target and inhibit the metastatic process.
- The absence of effective anti-metastasis drugs is partly attributed to a lack of suitable preclinical models for screening and development.
Purpose of the Study:
- To highlight the critical role of metastasis in cancer patient mortality.
- To introduce and advocate for the use of established tumor cell migration screening models.
- To propose the evaluation of both novel and existing drugs for their anti-metastasis potential using these models.
Main Methods:
- Utilizing established in vitro and/or in vivo models that accurately recapitulate tumor cell migration.
- Employing these models as a surrogate for metastasis formation in drug screening assays.
- Testing a range of compounds, including novel drug candidates and established drugs from various therapeutic areas.
Main Results:
- Demonstrated the utility of tumor cell migration assays as reliable surrogates for evaluating anti-metastasis efficacy.
- Provided evidence supporting the potential of certain compounds to inhibit cancer cell migration.
- Identified a rationale for repurposing existing drugs and developing novel agents targeting metastasis.
Conclusions:
- Tumor cell migration assays represent a significant advancement in the development of anti-metastasis therapies.
- Both novel and established drugs warrant investigation for their ability to inhibit cancer metastasis.
- Targeting cancer cell migration offers a promising therapeutic strategy to combat metastasis-driven cancer mortality.
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