Cellular signaling pathways implicated in metastasis of colorectal cancer and the associated targeted agents
Xuan Liu1, Qing Ji1, Zhongze Fan2
1Department of Medical Oncology, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, PR China.
Abstract:
Colorectal cancer (CRC) is the third leading cancer worldwide and CRC-related death is mainly attributed to metastasis. Many cellular signaling pathways have been demonstrated to be aberrant in colorectal tumors, and some of them lead to the acquisition of malignant phenotypes. Therefore, the evaluation of signaling pathways implicated in CRC metastasis is urgent for further understanding of CRC progression and pharmacotherapy. This review focuses on several novel cellular signaling pathways associated with CRC metastasis, including Wnt/β-catenin, p53, COX, TGF-β/Smad, NF-κB, Notch, VEGF and JAKs/STAT3 signaling pathways. Targeted agents developed based on these pathways are also briefly discussed.
Insights
Colorectal cancer (CRC) metastasis is a major cause of death. This review explores novel cellular signaling pathways like Wnt/β-catenin and VEGF that drive CRC progression and potential targeted therapies.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Colorectal cancer (CRC) is a leading global cause of cancer-related mortality.
- CRC-related deaths are predominantly linked to metastatic disease.
- Aberrant cellular signaling pathways are implicated in the development of malignant phenotypes in colorectal tumors.
Purpose of the Study:
- To review novel cellular signaling pathways involved in colorectal cancer (CRC) metastasis.
- To enhance understanding of CRC progression mechanisms.
- To discuss targeted agents for CRC pharmacotherapy.
Main Methods:
- Literature review of cellular signaling pathways in CRC metastasis.
- Focus on Wnt/β-catenin, p53, COX, TGF-β/Smad, NF-κB, Notch, VEGF, and JAKs/STAT3 pathways.
- Brief discussion of targeted agents based on these pathways.
Main Results:
- Several key signaling pathways (Wnt/β-catenin, p53, COX, TGF-β/Smad, NF-κB, Notch, VEGF, JAKs/STAT3) are critically involved in CRC metastasis.
- These pathways contribute to the acquisition of malignant phenotypes driving cancer progression.
- Targeted therapeutic strategies are being developed based on these identified pathways.
Conclusions:
- Understanding aberrant signaling pathways is crucial for combating CRC metastasis.
- Novel therapeutic targets offer promise for improved CRC treatment and patient outcomes.
- Further research into these pathways can refine pharmacotherapy for colorectal cancer.
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