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Related Concept Videos

Cancer Survival Analysis01:21

Cancer Survival Analysis

Cancer survival analysis focuses on quantifying and interpreting the time from a key starting point, such as diagnosis or the initiation of treatment, to a specific endpoint, such as remission or death. This analysis provides critical insights into treatment effectiveness and factors that influence patient outcomes, helping to shape clinical decisions and guide prognostic evaluations. A cornerstone of oncology research, survival analysis tackles the challenges of skewed, non-normally...
Treatment Resistant Cancers02:56

Treatment Resistant Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
Truncation in Survival Analysis01:09

Truncation in Survival Analysis

Truncation in survival analysis refers to the exclusion of individuals or events from the dataset based on specific criteria related to the time of the event. This exclusion can happen in two primary forms: left truncation and right truncation.
Left truncation occurs when individuals who experienced the event of interest before a certain time are not included in the study. This is often due to a "delayed entry" into the study where only those who survive until a certain entry point are observed.
Tumor Progression02:07

Tumor Progression

Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Tumor Progression02:07

Tumor Progression

Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
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Metastasis02:30

Metastasis

Metastasis is the spread of cancer cells from the original site to distant locations in the body. Cancer cells can spread via blood vessels (hematogenous) as well as lymph vessels in the body.
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...

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Tracking Tumor Cell Dissemination from Lung Metastases Using Photoconversion
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TRAILing death in cancer.

Gregory Mellier1, Sinong Huang, Kirthan Shenoy

  • 1Department of Physiology, Yong Loo Lin School of Medicine, Singapore.

Molecular Aspects of Medicine
|December 10, 2009
PubMed
Summary

Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) shows promise for cancer therapy by targeting cancer cells. Overcoming TRAIL resistance is key to improving treatment outcomes.

Area of Science:

  • Oncology
  • Molecular Biology
  • Immunology

Background:

  • Cancer cells often express death receptors (DRs) on their surface, making them targets for novel anti-cancer therapies.
  • Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is a promising molecule that selectively induces apoptosis in cancer cells by binding to DRs (TRAIL-R1/R2, DR4/DR5).
  • TRAIL-induced apoptosis involves both extrinsic and intrinsic pathways, regulated at multiple cellular levels.

Purpose of the Study:

  • To review the biology, function, and translational relevance of TRAIL in cancer therapy.
  • To discuss mechanisms of TRAIL resistance in cancer cells.
  • To explore strategies for overcoming TRAIL resistance to improve therapeutic efficacy.

Main Methods:

  • Literature review focusing on TRAIL biology, apoptosis pathways, and resistance mechanisms.

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  • Analysis of current research trends in overcoming TRAIL resistance.
  • Evaluation of translational relevance and clinical implications.
  • Main Results:

    • TRAIL demonstrates tumor-selective apoptosis induction via death receptor ligation.
    • TRAIL-induced apoptosis is regulated at both cell surface and intracellular levels.
    • Cancer cells can develop resistance to TRAIL, posing a significant therapeutic challenge.

    Conclusions:

    • Understanding TRAIL resistance mechanisms is crucial for effective cancer treatment.
    • Developing strategies to overcome TRAIL resistance is essential for improving clinical outcomes.
    • TRAIL-based therapies hold significant potential if resistance issues are addressed.