Synthetic Biomarkers May Aid in Early Detection of Ovarian Cancer

Early Treatment of Ovarian Cancer is Important

Ovarian cancer is notoriously difficult to detect in the early stages, resulting in poor survival rates for patients. MIT engineers have developed a synthetic biomarker that could detect ovarian tumors five months earlier than current testing methods.

Early Cancer Treatment of Ovarian Tumors

Five-year survival rates surpass 90 percent when ovarian cancer is detected early. Unfortunately, the disease is usually asymptomatic in the earlier stages. Any symptoms that do present tend to be non-specific, such as fatigue and weight loss.

Current testing looks for the presence of blood biomarkers produced by ovarian tumors, but it can take eight to 10 years for them to reach a high enough concentration to be detected. Ultrasound imaging reveals only tumors that are at least one centimeter in diameter.

Synthetic vs. Natural Biomarkers

Synthetic biomarkers are nanoparticles that interact with tumor proteins. The process releases fragments that can be detected in a patient’s urine, resulting in a more accurate test than one conducted on natural biomarkers in the bloodstream.

Professor Sangeeta Bhatia and her team at MIT engineered a synthetic biomarker to be approximately 15 times better than a previous version. The nanoparticle was then tested against a blood biomarker in mice with ovarian cancer.

The synthetic biomarker was able to detect ovarian cancer composed of tumors as small as two millimeters in diameter. Researchers are now testing the possibility of using this method with other types of cancer.

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Targeted Cancer Drugs May Protect Fertility in Female Cancer Patients

There is New Hope for Cancer Patients.
There is New Hope for Cancer Patients to Have Children After Treatment

Women of child-bearing age who are undergoing cancer treatment are often vulnerable to infertility. Researchers recently discovered that a certain type of targeted cancer drug may block this unfortunate side effect of chemotherapy.

How Cancer Treatment Affects Fertility

Chemotherapy drugs work by targeting rapidly developing cells and damaging cellular DNA. Oocytes, or immature egg cells, are hypersensitive to DNA damage in order to “retain genomic fidelity.”

In addition, chemotherapy triggers a signaling pathway in the ovaries, resulting in premature maturation of primordial follicles. This process is often referred to as follicular burnout.

Currently there are two primary options for women to preserve their fertility while receiving chemotherapy:

• Goserelin (trade name Zoladex®) and leuprolide (trade name Lupron®) are drugs that temporarily shut down the ovaries.

• Cryopreservation involves harvesting eggs and freezing them for future use or fertilizing them outside the body and freezing the embryos.

Can Targeted Cancer Drugs Help to Preserve Fertility?

mTOR inhibitors have been approved for clinical use as they undergo continued testing for application as targeted cancer drugs. Since mTOR is a vital element in an ovary’s signaling pathway, researchers suspect that blocking the enzyme could protect the reserve of primordial follicles.

During the study, female mice who received chemotherapy only experienced follicular burnout, while those who received mTOR inhibitors as supplements maintained the reserves of primordial follicles. The latter also became pregnant at normal rates, while the former were primarily infertile.

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CAR T-Cells May Be an Effective Immunotherapy for Multiple Myeloma

Is Issels Genomic Testing for Personalized Treatment For You
Is Issels Genomic Testing for Personalized Treatment For You?

Researchers have been focusing on CAR T-cells as the basis for a promising immunotherapy cancer treatment. Recent trials show encouraging results for the use of CAR T-cells in fighting advanced multiple myeloma.

CAR T Cells: A New Approach in Cancer Treatment

Scientists are excited about CAR T-cell therapy because it uses a patient’s own immune cells to treat cancer. The cells are gathered from the patient’s blood, engineered to produce chimeric-antigen receptors (CARs), and multiplied in the lab to reach quantities in the billions.

At that point, the cells are reintroduced into the patient’s bloodstream, to where they attach themselves to specific targets on cancer cells. CAR T-cell products, currently awaiting FDA approval, target the CD19 antigen in leukemia and lymphoma.

Can CAR T-Cells Treat Different Cancers?

Two CAR T-cell trials were recently conducted in the United States and China. Results were presented last June at the annual meeting of the American Society of Clinical Oncology in Chicago.

Both trials examined the use of CAR T-cells that target B-cell maturation antigens (BCMA), which are proteins found in myeloma cells. Most of the patients in the studies achieved positive results, with many experiencing complete remission.

CAR T-cell research is still in the early stages. Testing will continue to validate these findings and determine whether CAR T-cell therapy is a viable treatment method for cancer patients.

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High Fat Diets Are Linked to Colon Cancer

High Fat Diets Are Linked to Colon Cancer
High Fat Diets Are Linked to Colon Cancer

Doctors regularly warn patients that obesity is linked to an increased risk of cancer. A study by researchers at MIT has shed some light on how high-fat diets can trigger colon cancer.

The Role of Stem Cells in Colon Cancer

Colon cancer arises from mutations that tend to accumulate among intestinal stem cells, which last a lifetime. Omer Yilmaz, an assistant professor of biology at MIT, led a team that set out to discover the process behind these cellular changes.

For nine months to a year, Yilmaz and his team fed healthy mice a diet composed of 60 percent fat. In addition to gaining up to 50 percent more body mass, these mice developed more intestinal tumors than those on a healthy diet.

Effects of High-Fat Diet on Intestinal Cells

Researchers observed significant changes in the intestinal stem cells of the mice:

  • The mice eating a high-fat diet had a higher number of intestinal stem cells. In addition, they were able to operate free of input from niche cells that normally regulate stem cell activity.
  • Progenitor cells, which are differentiated “daughters” of stem cells, began to take on characteristics of stem cells, including longer life span and ability to generate mini-intestines outside the body.

Yilmaz is hopeful that, with further investigation, this information will lead to identifying new methods of cancer treatment for obesity-related tumors.

The Issels® Difference: Non-Toxic, Personally Tailored Cancer Treatment

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Molecularly Targeted Therapy – Considered Exciting Cancer News

Molecular Targeted Therapy Hit the Bulls Eye!
Molecular Targeted Therapy Hit the Bulls Eye!

Traditional cancer treatments often attack both cancer and healthy cells, resulting in debilitating side effects such as fatigue and weight loss. Doctors are excited about a revolutionary cancer treatment that specifically targets cancer cells.

Cancer Treatment that “Hits the Bullseye”

As implied by the name, molecularly targeted therapy involves drugs designed at the molecular level of the cell to attack and destroy specific types of cancer. Glivec (or Gleevec), also known as STI571, is the pioneering drug in this promising new therapy.

These so-called “designer drugs” begin with the identification of an abnormal molecule unique to a particular type of cancer. Scientists can then create a drug that interferes with the function of that molecule.

Glivec: Targeting Leukemia

Glivec has been found to be effective against chronic myeloid leukemia, also known as CML. Dr. Brian Druker, who led the research on Glivec, discovered that scientists have previously used STI571 to treat a rare gastrointestinal cancer that shares an enzyme related to one in CML.

Dr. Druker, who also serves as director of the leukemia program at the Oregon Health Sciences University, believes that STI571 can lead the way in finding the abnormalities in other types of cancer so they can also be treated with molecularly targeted therapy.

FDA approval of Glivec was fast-tracked and the drug is now available from Novartis Pharmaceuticals.

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Tips for Lowering Your Stress Levels While in Cancer Treatment

Taking a Deep Breath and Seeking Help Can Really Help Take Stress Down a Notch.
Taking a Deep Breath and Seeking Help Can Really Help Take Stress Down a Notch.

If you have been diagnosed with cancer, stress relief is more important than ever for your quality of life. A recent study found that relaxation techniques such as yoga and meditation actually produce molecular changes that counteract depression.

The Immune System in Overdrive

When stress triggers the familiar “fight-or-flight” reaction, it also boosts production of a molecule called NF-kB. This molecule in turn stimulates genes to produce cytokines, which are proteins that cause inflammation as part of the immune system response.

In the short term, this process is helpful in battling infections and other common ailments. Problems arise when the pro-inflammatory gene expression is chronic, leading to higher cancer risk along with accelerated aging and mental disorders such as depression.

Exploring the Mind-Body Connection

The study from the Universities of Coventry and Radboud, published in Frontiers in Immunology, examined gene behavior in 846 participants over a span of 11 years. Principle focus was the effect of mind-body interventions (MBIs) such as yoga, tai chi and meditation.

Results showed that regular practice of MBIs caused reduced production of NF-kB and cytokines. This decrease reversed the pro-inflammatory gene expression pattern, with a corresponding reduction in the risk of inflammation-related conditions.

According to lead researcher Ivana Buric, the process leaves a “molecular signature” that reverses the effects of stress and anxiety. MBIs can change the genetic code to follow a path toward health and well-being.

Immunotherapy for Cancer: A Personalized Approach

No two cases of cancer are the same. Contact us to learn how Issels® uses individually developed immunotherapy for cancer programs to help patients of all ages and all forms of cancer.