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Published on: November 28, 2019
Role of the tumor microenvironment in regulating apoptosis and cancer progression
Katherine Yaacoub1, Remy Pedeux2, Karin Tarte3
1Université Rennes 1, 2 Av. du Pr Léon Bernard, Rennes Cedex 35043, France; UMR INSERM, 917, 2 Av. du Pr Léon Bernard, Rennes Cedex 35043, France; INSERM ER440-OSS, CLCC Eugène Marquis, Rue Bataille Flandres Dunkerque, Rennes 35042, France.
Abstract:
Apoptosis is a gene-directed program that is engaged to efficiently eliminate dysfunctional cells. Evasion of apoptosis may be an important gate to tumor initiation and therapy resistance. Like any other developmental program, apoptosis can be disrupted by several genetic aberrations driving malignant cells into an uncontrolled progression and survival. For its sustained growth, cancer develops in a complex environment, which provides survival signals and rescues malignant cells from apoptosis. Recent studies have clearly shown a wide interaction between tumor cells and their microenvironment, confirming the influence of the surrounding cells on tumor expansion and invasion. These non-malignant cells not only intensify tumor cells growth but also upgrade the process of metastasis. The strong crosstalk between malignant cells and a reactive microenvironment is mediated by soluble chemokines and cytokines, which act on tumor cells through surface receptors. Disturbing the microenvironment signaling might be an encouraging approach for patient's treatment. Therefore, the ultimate knowledge of "tumor-microenvironment" interactions facilitates the identification of novel therapeutic procedures that mobilize cancer cells from their supportive cells. This review focuses on cancer progression mediated by the dysfunction of apoptosis and by the fundamental relationship between tumor and reactive cells. New insights and valuable targets for cancer prevention and therapy are also presented.
Insights
Cancer cells evade apoptosis, a programmed cell death, to survive and grow. Understanding the tumor microenvironment
Area of Science:
- Oncology
- Cell Biology
- Cancer Research
Background:
- Apoptosis is a crucial cellular process for eliminating damaged cells, and its evasion is linked to cancer initiation and treatment resistance.
- Cancer cells exploit their surrounding microenvironment, receiving survival signals that promote uncontrolled growth, invasion, and metastasis.
- The interaction between tumor cells and their microenvironment is mediated by complex signaling pathways involving chemokines and cytokines.
Purpose of the Study:
- To review the role of apoptosis dysfunction in cancer progression.
- To explore the intricate relationship between tumor cells and their reactive microenvironment.
- To identify novel therapeutic targets and strategies for cancer prevention and treatment.
Main Methods:
- This review synthesizes current research on apoptosis and tumor microenvironment interactions.
- It analyzes genetic aberrations affecting apoptosis in cancer development.
- It examines the signaling crosstalk between malignant and non-malignant cells.
Main Results:
- Evasion of apoptosis is a key mechanism enabling tumor initiation and therapy resistance.
- The tumor microenvironment actively supports cancer cell survival, proliferation, and metastasis.
- Disrupting microenvironment signaling presents a promising therapeutic avenue.
Conclusions:
- Understanding the interplay between apoptosis evasion and the tumor microenvironment is critical for advancing cancer therapy.
- Targeting the tumor microenvironment can disrupt cancer progression and metastasis.
- Further research into these interactions will yield novel strategies for cancer prevention and treatment.
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