A new study published online Oct. 30 in Immunity, a Cell Press publication, reveals a cancer therapy technique that researchers describe as more accurate, long-lasting, and less harmful than current treatments.
Published Date – 06:01 PM, Sat – 4 November 23
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Washington: For far too long, cancer treatment has been a double-edged sword, with treatments designed to target cancer cells sometimes harming healthy cells as well.
A new study published online Oct. 30 in Immunity, a Cell Press publication, reveals a cancer therapy technique that researchers describe as more accurate, long-lasting, and less harmful than current treatments.
The research, led by immunology researcher Jose Ramon Conejo-Garcia, MD, PhD at Duke University School of Medicine, focuses on the novel use of IGA antibodies to target and kill tumor-promoting molecules found deep within cancer cells, which have previously eluded existing treatment options, including IGA antibody treatment.
“This is a proof-of-concept study, but the results are very promising,” said Conejo-Garcia, a Duke Science and Technology scholar in the Department of Integrative Immunobiology. “We believe that this treatment could be used to target a wide range of cancer mutations.” Early experiments on mice with lung and colon cancer revealed notable reductions in tumor growth and minimal side effects.
The study focused on a particular type of antibody called dimeric IgA (digA). Its special structure allows it to target specific mutations linked with PIGR, a protein expressed on the surface of virtually all epithelial cancer cells that contributes to the growth and survival of cancer cells.
One such mutation, KRAS G12D, is a known instigator of the deadliest cancers. The study revealed that digA binds to rogue, mutated proteins then ushers them out of the cell in a process called transcytosis, stopping tumor growth.
When tested in mice, the KRAS G12D-specific antibody was more effective at shrinking cancer tumors than current treatments in clinical tests. Small molecule treatments often struggle to reach certain cancer cells, have short-half lives, and can cause side effects.
Researchers found similar results with another cancer mutation, IDH1 R132H, found deep inside cancer cells.
Scientists have struggled to target the mutated KRAS protein, but the new findings suggest the uniquely designed antibody can reach these intracellular molecules.
According to researchers, IGA antibodies have the potential for use as targeted therapy against stubborn mutations driving common, aggressive cancers, particularly epithelial cancers such as ovarian, skin, colon, cervical, prostate, breast, and lung cancer.
“This is a new way of targeting tumor cells by using an antibody that is exquisitely specific for point mutations or molecules that are truly tumor specific,” said Conejo-Garcia. “By neutralizing them and ensuring these tumor-promoting molecules are expelled outside the cell, we can halt tumor growth.” Throughout his career, Conejo-Garcia has researched ways to make our body’s defense system, the immune system, better at fighting certain cancers.
Conejo-Garcia worked on the current study with post-doctoral fellows Subir Biswas, PhD; Gunjan Mundal, PhD; and Carmen Maria Anandon, PhD, co-senior authors of the study, while at H. Lee Moffitt Cancer Center and Research Institute, and finalized the research after he joined the Duke faculty in 2023.The results offer a glimpse of future cancer treatments that are more tailored, reducing harm to healthy cells and improving patients’ quality of life.
IGA antibodies are just one part of the innovative field of immunotherapy. Treatments like PD-1 inhibitors and CAR T-cells have shown unprecedented durable cancer remissions.
“The immune system is the only system in the body that has two key properties that make it ideal for cancer treatment: specificity and memory,” said Conejo-Garcia, a member of the Duke Cancer Institute. The immune system can specifically target tumor cells and it can also remember those cells to mount a more effective attack if the cancer returns.
