The secrets of life lie in the molecular flexibility.
Welcome to Prof. Mariusz Jaremko's research group, the
Flexible Systems Lab!
Untangling untidy folds to understand diseases
Copper ions could play a key role when peptide folding goes wrong and leads to harmful aggregates.
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Picking the best methods for metabolomics research
Comparison of different nuclear magnetic resonance spectroscopy methods has helped to identify the most robust approach for studying different types of biomolecules.
Surgery, chemotherapy, and radiation are standard cancer therapies to remove or kill cancer cells. These therapies can successfully treat cancer in its early stages but are typically less effective at advanced stages or recurrence. The past few decades have led to a fourth therapy, cancer immunotherapy. Among the immunotherapy approaches for tumors is cancer vaccination. Cancer vaccines can stimulate immunity against tumors through tumor antigens. Ideal cancer vaccines stimulate both cellular and humoral immunity while overcoming tumor-immune suppression to stop tumor growth and eventually kill tumor cells. Cancer vaccines are different from conventional vaccines since their therapeutic goals involve triggering tumor antigen-specific cellular immune responses to destroy the tumor cells. Additionally, tumor antigens are endogenous and have limited immunogenicity, unlike conventional vaccinations that use antigens from exogenous infections.
Although the identification and characterization of several tumor antigens have led to the creation of numerous antigen-derived cancer vaccines, many vaccines lack clinical effectiveness because they are insufficiently immunogenic. Therefore, adjuvants are used in vaccination formulations to promote potent and durable immune responses. In this chapter, we summarize the current standard cancer treatment modalities, highlight the present state of cancer immunotherapy, and describe many platforms and optimization techniques for cancer vaccines.