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In the previous text we talked about the importance of early diagnosis as one of the main allies for the cure of colorectal cancer. Now let’s talk about a great advance in science in the search for more efficient and less aggressive treatments than conventional chemotherapy and radiotherapy, used in the vast majority of cases.

Recently, a group of researchers from Germany published promising results from the application of a protective vaccine against hereditary colorectal cancer in mice. This type of colorectal cancer accounts for about 3% of cases (1 in 30) and is caused by an inherited syndrome called Lynch Syndrome.

In this study, scientists at the University Hospital of Heidelberg, Germany, identified that many patients with this syndrome had identical mutations in the DNA of the cancer cell. “The most interesting thing is that four of these mutations had the ability to make the body’s own defense cells attack the tumor”; account Dr. Carolina Melo, researcher at the Translational Research Laboratory of the Study and Research Nucleus (NEP).

They then developed a vaccine with proteins containing these mutations to be tested in mice. According to Dr. Carolina, it’s as if the vaccine showed the mouse’s defense cells which defective cells must be eliminated and so they attack the cancer as soon as it appears.

“The vaccinated mice survived longer and had a significantly smaller tumor than the unvaccinated ones. It was the first time that tests in a living being showed that it is possible to delay the development of hereditary colorectal cancer with a vaccine developed from mutations found in the cancer cell”; emphasizes the researcher.

Clinical trials demonstrating the safety and immunological efficacy of this vaccination in humans have already been successfully completed in a hospital in Frankfurt, Germany, and in the coming years we will know if it will be able to prevent tumors and prolong patient survival.

Science and medicine are doing their part in finding more efficient ways to treat and prevent colorectal cancer. Make you yours too! Beware! Make your routine exams according to medical advice, have healthy eating habits, exercise. Take care of yourself!

• Text written by Dr. Carolina Melo, PhD in human genetics, who has been working for over 10 years in oncology research and is currently part of the NEP research team.

Colorectal cancer, despite being the second most common type of cancer in men and women (apart from non-melanoma skin cancer), is also one of the most preventable. That’s because he doesn’t suddenly appear. This type of cancer originates from polyps (abnormal cell growth) located in the large intestine in the colon, rectum and anus regions. They usually don’t cause symptoms and can take between 10 and 15 years to develop into cancer. But if detected during a colonoscopy (a test that captures real-time images of the intestine) they can be removed before cancer occurs.

However, only 40% of colorectal cancer cases are detected at an early stage. The vast majority are detected in advanced stages, when symptoms are more evident and existing treatments less effective.

But if there are ways to diagnose it early, why is it still happening? According to the doctor. Carolina Melo, a researcher at the NEP’s Translational Research Laboratory, one of the main reasons is that there is still a lot of prejudice against colonoscopy, as it is an invasive technique, which requires a preparation (cleaning) of the colon considered unpleasant because it includes the use of laxatives and large water intake.

Routine colonoscopy should be performed in the population, in general, from 50 years of age, with regular intervals that can go from 3 to 5 years, according to medical advice.

“If everyone was aware of the suffering that can be avoided with the early diagnosis of colorectal cancer, there might not be room for this type of prejudice. There are other ways to screen for signs of colorectal cancer, but colonoscopy is the only one that can prevent it from starting by removing the polyps”; emphasizes Dr. Carolina.

Some people have a higher risk of getting this disease. About 3% of cases (1 in 30) of colorectal cancer are caused by an inherited syndrome called Lynch Syndrome. In this syndrome, mutations in genes that help repair DNA damage can increase by up to 50% a person’s risk of developing colorectal cancer, usually relatively young. Therefore, knowing the family history is very important in these cases.

In addition, for those who have problems with intestinal inflammation, such as Crohn’s disease and ulcerative colitis, or have a first-degree relative who has already had some type of bowel cancer, this test should start from 40 years of age onwards. .

The good news is that researchers are working on the search for biomarkers, such as specific cells, molecules or genes, that allow the early diagnosis of cancer in a less invasive and more assertive way. Another advance in colorectal cancer treatment is the recent publication of promising results from the application of a protective vaccine against hereditary colorectal cancer in mice.

Want to learn more about scientific advances in the diagnosis and treatment of colorectal cancer? In the next edition, Dr. Carolina continues talking about this topic on our social networks and on Infoco.

• Text written by Dr. Carolina Melo, PhD in human genetics. She has worked for over 10 years in oncology research and is currently part of the NEP research team.

The Pink October campaign – prevention of breast cancer – highlights the importance of an early and effective diagnosis for all audiences. This type of cancer affects 2.2 million women worldwide and, in Brazil, it is responsible for approximately 18 thousand deaths per year. Did you know that IMP has a team of researchers looking for new ways to help diagnose and treat breast cancer patients? The group at the Center for Studies and Research (NEP) has been working to find a more accurate and less invasive diagnosis.

One of the proposals developed at the Laboratory of Translational Research in Oncology at NEP is carried out by doctoral student Thayse Batista, in collaboration with Fiocruz Minas. Thayse is studying the profile of tumor microvesicles present in the blood of breast cancer patients treated at Hospital Luxembourg. These microvesicles are released by the tumor and immune system cells and are present in the blood. According to Thayse, the goal is to develop a diagnosis using microvesicles, which are structures released by the tumor since its formation, when it is still difficult to detect by imaging, making this method less invasive and efficient in detecting the disease and monitoring the treatment .

“The microvesicles carry several characteristic molecules of the tumor, which allows the identification of its origin and communication with other organs. One of the functions of these microvesicles is to allow the tumor to grow and develop in other organs, causing metastasis, as its release reaches other organs through the blood and transforms it into a favorable environment for tumor growth”; explains.

Knowing in depth how the tumor relates to the body is a powerful tool in the fight against breast cancer and providing this type of personalized treatment for SUS patients is an advance in quality health care for all. .

The work developed by Thayse has the collaboration of the clinical team of mastology and oncology, the NEP researchers and the patients who accept to participate in the Center’s research.

Thayse highlights that working closely with breast cancer patients has brought a new perspective to my work. “Meeting these women who face this disease, often with a smile on their faces, inspires me every day to seek more diligently for a service that will make this journey more peaceful and effective.”

*Text written by the Study and Research Center (NEP) team