How do cancer therapies often take advantage of altered cellular regulation?

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Cancer therapies often take advantage of altered cellular regulation primarily by targeting specific pathways that are dysregulated in cancer cells. Cancer cells frequently exhibit abnormal regulation of various signaling pathways that control growth, division, and survival. These alterations can lead to uncontrolled proliferation and resistance to normal regulatory mechanisms, creating unique vulnerabilities that can be exploited.

For instance, therapies may focus on inhibiting overactive signaling pathways that are essential for cancer cell survival or proliferation. This could involve using targeted therapies that block specific proteins or receptors that are frequently overexpressed or mutated in cancerous cells. By selectively targeting these dysregulated pathways, treatments can effectively disrupt the cancer cell’s ability to grow and survive, while minimizing damage to normal cells.

Other options do not align as closely with the principles of targeted cancer therapy. Enhancing the metabolic functions of normal cells does not directly address the specific vulnerabilities of cancer cells. Promoting apoptosis in all cells lacks the nuance required to distinguish between healthy and cancerous cells, which can result in significant side effects and damage to normal tissues. Finally, while repairing damaged DNA in cancer cells can be a component of some treatments, it is not a primary strategy in most cancer therapies; rather, many treatments aim to induce further damage to prevent cancer cells from proliferating

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