Unique Monoclonal Antibody Can Recognize A Cancer-Associated Protein Inside A Cell And Destroy It

Main Category: Cancer / Oncology
Also Included In: Lymphoma / Leukemia / Myeloma
Article Date: 17 Mar 2013 - 2:00 PDT



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Unique Monoclonal Antibody Can Recognize A Cancer-Associated Protein Inside A Cell And Destroy It

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Researchers have discovered a unique monoclonal antibody that can effectively reach inside a cancer cell, a key goal for these important anticancer agents, since most proteins that cause cancer or are associated with cancer are buried inside cancer cells. Scientists from Memorial Sloan-Kettering Cancer Center and Eureka Therapeutics have collaborated to create the new human monoclonal antibody, which targets a protein associated with many types of cancer and is of great interest to cancer researchers.

Unlike other human therapeutic monoclonal antibodies, which can target only proteins that remain on the outside of cancer cells, the new monoclonal antibody, called ESK1, targets a protein that resides on the inside of the cell.

ESK1 is directed at a protein called WT1, which is overexpressed in a range of leukemias and other cancers including myeloma and breast, ovarian, and colorectal cancers. WT1 is a high priority target for cancer drugs because it is an oncogenic protein, meaning that it supports the formation of cancer. In addition, it is found in few healthy cells, so there are less likely to be side effects from drugs that target it.

"This is a new approach for attacking WT1, an important cancer target, with an antibody therapy. This is something that was previously not possible," said David A. Scheinberg, MD, PhD, Chair of the Sloan-Kettering Institute's Molecular Pharmacology and Chemistry Program and an inventor of the antibody. "There has not been a way to make small molecule drugs that can inhibit WT1 function. Our research shows that you can use a monoclonal antibody to recognize a cancer-associated protein inside a cell, and it will destroy the cell."

The first studies of the antibody are showing promise in preclinical research as a treatment for leukemia as reported March 13, 2013, in Science Translational Medicine.

"ESK1 represents a paradigm change for the field of human monoclonal antibody therapeutics," said Cheng Liu, PhD, President and Chief Executive Officer of Eureka Therapeutics. "This research suggests that human antibody therapy is no longer limited to targeting proteins present outside cancer cells, but can now target proteins within the cancer cell itself."

ESK1 was engineered to mimic the functions of a T cell receptor, a key component of the immune system. T cells have a receptor system that is designed to recognize proteins that are inside the cell. As proteins inside the cell get broken down as part of regular cellular processes, molecules known as HLA molecules carry fragments of those proteins - known as peptides - to the surface. When T cells recognize certain peptides as abnormal, the T cell kills the diseased cell.

In the current study, the investigators showed that ESK1 alone was able to recognize WT1 peptides and kill cancer cells in the test tube and also in mouse models for two different types of human leukemia. "We were surprised that the antibody worked so well on its own," said Dr. Scheinberg, senior author of the paper. "We had originally expected that we might need to use the antibody as a carrier to deliver a drug or a radioactive therapy to kill the cancer cells, but this was not necessary."

Additional studies must be done in the laboratory before ESK1 is ready to be tested in patients. But the monoclonal antibody was engineered to be fully human, which should speed the time it takes to move the drug into the clinic. Researchers expect that the first clinical trials, for leukemia, could begin in about a year.

The antibody was developed under a collaborative effort between Memorial Sloan-Kettering and Eureka, which have jointly filed for patent protection.

Article adapted by Medical News Today from original press release. Click 'references' tab above for source.
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This work was supported by grants from the Leukemia and Lymphoma Society, the National Cancer Institute, the Sloan-Kettering Institute's Experimental Therapeutics Center and Technology Development Fund, the Commonwealth Foundation for Cancer Research, the Tudor and Glades Foundations, the Merker Fund, the Lymphoma Foundation, and the Mesothelioma Applied Research Foundation.
Memorial Sloan-Kettering Cancer Center
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Visitor Opinions (latest shown first)

Ingenious approach to kill the devil in cancer

posted by Oliver Birnso on 18 Mar 2013 at 8:29 pm

Ingenious approach to kill the devil in cancer.

In response to Greg's comment above, this antibody does not actually enter the cell but rather it targets a peptide which is normally processed inside the cancer cell from an internal protein, and then comes out to the cell surface, delivered by the Major Histocompatibility complex(MHC) or HLA, which has direct contact with exterior of the cell. The engineered antibody, if delivered outside the cell, will then react with the cell surface-delivered peptide(antigen) and this will result in cancer cell death.

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Will the monoclonal antibody ever reach inside the "individual" cancer cell?

posted by Greg Pawelski on 17 Mar 2013 at 2:45 pm

It may be very important to zero in on different proteins. However, when actually taking the "targeted" drug, will it even enter the cancer cell? Once entered, does it immediately get metabolized or pumped out, or does it accumulate? In other words, will it work for every individual patient that tested positive for the target?

Simply having a target (even inside the cell) doesn't ensure that the drug will work. The drug might not get inside the cell at all. The drug can get pumped out of the cell. The drug can be inactivated by the cell. The cell can recover from the damage called by the drug by repairing damage or shutting down the cell death pathway or whatever.

All the validations of this protein or that protein provides us with a variety of sophisticated techniques to provide new insights into the tumorigenic process, but if the "targeted" drug either won't "get in" in the first place or if it gets pumped out/extruded or if it gets immediately metabolized inside the cell, it just isn't going to work.

Metabolism is the principal driver of human cancer. Cells speak to each other and the messages they send are interpreted via intracellular and intercellular pathways. You wouldn't know this using analyte-based proteomic methodologies. However, functional phenotype analysis can provide the window by testing various cell-death signaling pathways upstream and downstream.

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the end of chemo

posted by dr steve on 16 Mar 2013 at 11:04 am

Finally, we're seeing a glimmer of the the post-chemotherapy era. Congrats!

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