Molecular oncology

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Molecular oncology is an

tumors at the molecular scale. Also the development and application of molecularly targeted therapies
.

Main branches

Molecular oncology has identified genes that are involved in the development of cancer. The research combined diverse techniques ranging from

targets for novel chemotherapy drugs and other cancer treatments, or imaging scans. Scientists use a range of techniques to validate the role of the novel candidate genes in the development of cancer. The ultimate aim is to translate these findings into improved treatment options for cancer patients.[1]

Gene targets

There are many different genes being researched for possible cancer therapies. Among the most studied are the

tumor suppressors because their pathways oversee the repair of cells that may replicate out of control with damaged genetic material, eventually leading to cancer growth if not kept in check.[4] Mutations in these genes are seen in more than half of human cancers.[2]

Molecular oncolytic therapies

Immunotherapy

Immune gene therapy is a targeted approach to cancer therapy where actual immune cells of the patient and their genes are manipulated to produce an anti-tumor response.[5] The body's own immune system is used to attack the tumor cells, therefore the immune system can naturally attack the specific cancer cells again to in the future if necessary.[6] Many types of immunotherapies exist including bone marrow transplants, antibody therapies, and various manipulations of host immune cells to target and kill cancer cells. Cellular receptors, antigens, and cofactor molecules are some such cellular manipulations to target cancer cells.[5]

Chimeric antigen receptor T Cell

Chimeric antigen receptor T cell immunotherapy (CAR-T), possibly combined with cytokines and checkpoint inhibitors, are a regularly used form of immune gene therapy.[5] CAR-T involves manipulation of a patient's natural T cells to express a chimeric antigen receptor. This receptor, now on millions of the patient's T cells, recognizes cancerous cells that express specific antigens.[5] Usually, the T cell antigen receptor is inactive but when the receptor recognizes a certain cancerous antigen, the physical structure of the T cell changes to destroy the cancer cell.[7]
This is a method of cancer treatment that works on the cellular and molecular level.

Combining CAR-T with checkpoint inhibitors, cytokines

Some regulatory proteins, specifically immune checkpoint inhibitors, have been found to reduce the ability of T cells to multiply within the body.[7] In order to optimize the efficacy of CAR-T gene therapy, these checkpoint inhibitors can be blocked to stimulate a robust anti-tumor immune response, spearheaded by the CAR-T cells.[7] There are various known inhibitory receptors on the CAR-T cell; through manipulation of these receptors and the molecules that bind them, expression of the CAR-T cell can be amplified.[7]

CAR-T cells can also be combined with cytokines to improve the efficacy of the immunotherapy method.[7] Cytokines are messenger molecules that can act on themselves, nearby cells, or distant cells.[7] The signal pathways of these cytokines can be used to enhance CAR-T anti-tumor characteristics.[7] For example, Interleukin 2 (IL2) is a cytokine that acts as a growth factor for various immune system cells, including T cells. In regards to gene therapy, IL2 can be used to increase replication and dispersing of CAR-T cells throughout the body.[7]

Issues with CAR-T therapy

There is room for improvement with this gene therapy approach. Firstly, the antigens of interest expressed on the cancer cells may sometimes be expressed on regular body cells, too.

pro-inflammatory factors are released by the immune system and can cause unpleasant side effects for the patient like nausea and a high fever.[5]

Gene therapy

In the past few decades, gene therapy has emerged as a targeted way to treat cancer. Gene therapy introduces foreign genetic sequences to diseased cells in order to change the expression of these cancerous cells that are functioning with severely damaged genomes.[5] Cancer cells do not behave like normal cells, so the methods for ridding the body of these cells are more complicated. Manipulation of the pathways controlled by certain genes and their regulators are a large branch of cancer research.

See also

References