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Published on: June 20, 2015
Cancer plasticity in therapy resistance: Mechanisms and novel strategies
Xing Niu1, Wenjing Liu2, Yinling Zhang3
1China Medical University, Shenyang, Liaoning 110122, China; Experimental Center of BIOQGene, YuanDong International Academy Of Life Sciences, 999077, Hong Kong, China.
Abstract:
Therapy resistance poses a significant obstacle to effective cancer treatment. Recent insights into cell plasticity as a new paradigm for understanding resistance to treatment: as cancer progresses, cancer cells experience phenotypic and molecular alterations, corporately known as cell plasticity. These alterations are caused by microenvironment factors, stochastic genetic and epigenetic changes, and/or selective pressure engendered by treatment, resulting in tumor heterogeneity and therapy resistance. Increasing evidence suggests that cancer cells display remarkable intrinsic plasticity and reversibly adapt to dynamic microenvironment conditions. Dynamic interactions between cell states and with the surrounding microenvironment form a flexible tumor ecosystem, which is able to quickly adapt to external pressure, especially treatment. Here, this review delineates the formation of cancer cell plasticity (CCP) as well as its manipulation of cancer escape from treatment. Furthermore, the intrinsic and extrinsic mechanisms driving CCP that promote the development of therapy resistance is summarized. Novel treatment strategies, e.g., inhibiting or reversing CCP is also proposed. Moreover, the review discusses the multiple lines of ongoing clinical trials globally aimed at ameliorating therapy resistance. Such advances provide directions for the development of new treatment modalities and combination therapies against CCP in the context of therapy resistance.
Insights
Cancer cell plasticity (CCP) drives therapy resistance by enabling tumor adaptation. Targeting CCP offers new strategies to overcome treatment failure and improve cancer patient outcomes.
Area of Science:
- Oncology
- Cancer Biology
- Molecular Medicine
Background:
- Therapy resistance is a major challenge in cancer treatment.
- Cancer cell plasticity (CCP) is increasingly recognized as a key mechanism underlying treatment failure.
- Tumor heterogeneity and adaptation to microenvironment changes contribute to resistance.
Purpose of the Study:
- To review the formation and mechanisms of cancer cell plasticity (CCP).
- To explore how CCP facilitates cancer cells' escape from therapy.
- To discuss novel therapeutic strategies targeting CCP and ongoing clinical trials.
Main Methods:
- Literature review of recent research on cancer cell plasticity and therapy resistance.
- Analysis of intrinsic and extrinsic factors driving CCP.
- Synthesis of information on clinical trials investigating CCP-targeting therapies.
Main Results:
- Cancer cell plasticity involves phenotypic and molecular alterations driven by microenvironment, genetic, and epigenetic factors.
- CCP allows cancer cells to reversibly adapt to dynamic conditions, promoting tumor heterogeneity and resistance.
- Mechanisms driving CCP include intrinsic cellular adaptability and extrinsic pressures from the tumor microenvironment.
Conclusions:
- Cancer cell plasticity is a critical driver of therapy resistance.
- Inhibiting or reversing CCP presents promising therapeutic avenues.
- Targeting CCP through novel treatment modalities and combination therapies holds potential for improving cancer treatment efficacy.
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