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Targeted therapy: its status and promise in selected solid tumors. Part II: Impact on selected tumor subsets, and
Sasha O Joseph1, Jennifer Wu, Franco M Muggia
1Division of Hematology and Oncology, New York University (NYU) School of Medicine, New York, New York 10016, USA.
Abstract:
This second article in our two-part series on targeted therapies in solid tumors covers the emergence of targeted therapies for the treatment of two common malignancies: lung cancer and breast cancer. In these two tumors, the identification of a promising target has led to successful preliminary applications, and eventually to further advances through drug development and the fine tuning of patient selection. As a result, the percentage of patients with breast or lung cancer who are benefiting from targeted agents has steadily increased, even if the majority are still treated with conventional cytotoxic regimens. We also review the latest therapeutic strategies for colorectal and gynecologic cancers--because these offer an instructive contrast. The curative regimens that have been developed for these two tumors--even those in more advanced stages--have included combinations of surgery and/or radiation with chemotherapy. The Cancer Genome Atlas has revealed complexities in the biology of these tumors that underscore the fact that reliance on selective DNA-damaging agents such as platinums, antimetabolites, and antimitotic agents will continue for some time. We conclude that the therapeutic progress that may arise from the study of molecular pathways will be due not only to the development of new targeted therapies, but also to a better understanding of older drugs developed empirically in the past. Taken together, these two types of advance illustrate the remarkable overall effect of modern cancer therapeutics' focus on tumor biology and tumor immunology.
Insights
Targeted therapies are improving lung and breast cancer treatment by targeting specific molecular pathways. Understanding tumor biology and immunology enhances both new targeted drugs and older chemotherapy agents.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Therapeutics
Background:
- Targeted therapies represent a significant advancement in solid tumor treatment, particularly for lung and breast cancers.
- While targeted agents show increasing benefit, conventional cytotoxic chemotherapy remains a primary treatment modality for many patients.
- Colorectal and gynecologic cancers serve as a contrast, with established curative regimens involving multimodal approaches.
Purpose of the Study:
- To review the emergence and impact of targeted therapies in lung and breast cancers.
- To contrast these advancements with treatment strategies for colorectal and gynecologic cancers.
- To explore how understanding molecular pathways and tumor biology influences therapeutic progress.
Main Methods:
- Review of current literature on targeted therapies in solid tumors.
- Analysis of treatment strategies for lung, breast, colorectal, and gynecologic cancers.
- Discussion of findings from The Cancer Genome Atlas on tumor biology.
Main Results:
- Targeted therapies have led to increased patient benefit in lung and breast cancers through improved drug development and patient selection.
- Conventional cytotoxic regimens remain essential, with ongoing reliance on DNA-damaging agents.
- Complex tumor biology necessitates continued use of established chemotherapeutic agents.
Conclusions:
- Therapeutic progress stems from both novel targeted therapies and a deeper understanding of established drugs.
- Modern cancer therapeutics increasingly focus on tumor biology and immunology for improved outcomes.
- Advances in understanding molecular pathways are crucial for future cancer treatment development.
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