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Updated: Aug 7, 2026

Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics
Published on: May 14, 2016
TRAIL and Bortezomib: killing cancer with two stones
Muhammad Zahid Qureshi1, Mirna Azalea Romero, Rukset Attar
1Department of Chemistry, GCU Lahore, Lahore, Pakistan
Abstract:
Cancer genomics and proteomics have undergone considerable broadening in the past decades and increasingly it is being realized that solid/liquid phase microarrays and high-throughput resequencing have provided platforms to improve our existing knowledge of determinants of cancer development, progression and survival. Loss of apoptosis is a widely and deeply studied process and different approaches are being used to restore apoptosis in resistant cancer phenotype. Modulating the balance between pro-apoptotic and anti-apoptotic proteins is essential to induce apoptosis. It is becoming more understood that pharmacological inhibition of the proteasome might prove to be an effective option in improving TRAIL induced apoptosis in cancer cells. Keeping in view rapidly accumulating evidence of carcinogenesis, metastasis, resistance against wide ranging therapeutics and loss of apoptosis, better knowledge regarding tumor suppressors, oncogenes, pro-apoptotic and anti-apotptic proteins will be helpful in translating the findings from benchtop to bedside.
Insights
Understanding cancer development requires knowledge of tumor suppressors and oncogenes. Pharmacological proteasome inhibition may enhance TRAIL-induced apoptosis in cancer cells, aiding treatment strategies.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Cancer genomics and proteomics have advanced, revealing insights into cancer development, progression, and survival.
- Loss of apoptosis is a critical hallmark of cancer, and restoring it is a key therapeutic goal.
- Understanding the balance of pro-apoptotic and anti-apoptotic proteins is crucial for inducing cancer cell death.
Purpose of the Study:
- To explore the potential of pharmacological proteasome inhibition in enhancing TRAIL-induced apoptosis in cancer cells.
- To highlight the importance of understanding tumor suppressors, oncogenes, and apoptosis-regulating proteins for cancer therapy.
- To bridge the gap between basic research findings and clinical applications in cancer treatment.
Main Methods:
- Utilizing advanced platforms like microarrays and high-throughput resequencing to analyze cancer determinants.
- Investigating the modulation of pro-apoptotic and anti-apoptotic protein balance.
- Examining the effects of pharmacological proteasome inhibition on cancer cell apoptosis.
Main Results:
- Pharmacological proteasome inhibition shows promise in improving TRAIL-induced apoptosis in cancer cells.
- Enhanced knowledge of key cancer-related proteins can inform therapeutic strategies.
- The study emphasizes the need for a deeper understanding of carcinogenesis, metastasis, and therapeutic resistance.
Conclusions:
- Modulating apoptosis is essential for overcoming cancer resistance.
- Pharmacological proteasome inhibition is a potential strategy to enhance cancer cell apoptosis.
- Translating benchtop findings on cancer-related proteins to clinical practice is vital for improving patient outcomes.
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