Preview

Breast Cancer

Good Essays
Open Document
Open Document
461 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Breast Cancer
Breast cancer detection for the prevention and treatment

Director of molecular diagnostics, Tianjin Cancer Hospital Center in JinPu said, genetic testing is through the blood, other body fluids or tumor tissue for gene sequences were detected and analyzed. Currently, breast cancer topped the incidence of female cancer, and lung cancer is the first cancer mortality rates for men and women, the incidence increased year by year, and getting younger and younger.

Breast cancer risk population genetic screening technique to detect only need to be provided by 5 ml of peripheral blood, can breast cancer susceptibility gene for six full-exon gene mutation, according to susceptibility gene mutation, gene mutation carriers to assess chance of developing breast cancer, pursuant to adopt appropriate preventive measures, so as to achieve the purpose of early prevention of breast cancer.

Lung cancer genetic testing, is the use of lung cancer patients, "green beans" the size of a tissue sample, using next-generation sequencing technology, the 14 genes in lung cancer hotspot areas driven deep sequencing to detect gene mutations drive, and as a basis to optimize the development of individualized cancer targeted drug treatment programs, thus promoting individual treatment of lung cancer.

Clinical director of the National Cancer Research Center, Tianjin Cancer Institute director Hao Xishan academician said of tumor molecular diagnostics and gene detection platform built technology, is an important way to achieve tumor control and patient personalized medicine, will bring two The major change, one individual targeted therapy, the second is the prevention of diseases that may occur.

According to test results carried out a risk assessment of clinical intervention

With respect to lung cancer genetic testing technology, focusing on the prevention of breast cancer in high-risk populations by genetic screening technology more public attention. So, what populations are

You May Also Find These Documents Helpful

  • Satisfactory Essays

    This article is completely relevant to society. Women everywhere want to get tested for mutations in the BRCA1 and BRCA2 genes. The possibility of misdiagnosis is too high with only one possible test. Patients end up spending way more than they should for a test that often is not covered by insurance. Gene patenting can also greatly affect us in the long run if more and more genes become patented. It limits the ability for other scientists to research and learn more about the genes and also means we can end up overpaying for every type of test in the future.…

    • 381 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Tay Sachs Research Paper

    • 1245 Words
    • 5 Pages

    Genetic testing can also be performed on parents before they conceive a child to determine whether they are carriers of the disease. This would be especially important if both parents were from high-risk populations to prevent families from going through this horrible experience.…

    • 1245 Words
    • 5 Pages
    Good Essays
  • Satisfactory Essays

    3.06 Mutations Essay

    • 553 Words
    • 3 Pages

    A woman's lifetime risk of developing breast cancer is approximately 12 percent, but there are certain BRCA mutations that increase the risk for women to 50-80 percent. For ovarian cancer a BRCA mutation means that a woman goes from a 1.4 percent risk to a 40-60 percent jump. What are BCRA1 and BCRA 2 mutations? The term BRCA itself stands for breast cancer susceptibility. BRCA1 and BRCA2 belong to a class of human genes that suppress tumors. If these genes mutate, then one is considered as having a hereditary risk of breast and ovarian cancer. The BRCA1 and BRCA2 mutation means that a woman has an increased risk of breast and/or ovarian cancer before menopause. Sometimes close family members were diagnosed with cancer at an early age also. These harmful mutations also increase the risk of cervical, colon, uterine, stomach, melanoma and gallbladder cancer. There are no standard criteria for who should be tested for the BRCA gene mutation, but if you have family members who have had cancer, it is a definite clue. If any of these family members were young; before menopause, it is a good idea to think about being testing for the gene. It would be a very good idea to ask the family member to test for the BRCA mutation, so that the rest of the family members would know ahead of time also. According the National Cancer Institute, the risk of having the mutation is higher if you are of Ashkenazic Jewish descent. If this is the case, pay attention to if a parent or sibling has been diagnosed with cancer. Also, find out if any grandparents, half-siblings, nieces or nephews had cancer. Pay special attention to relatives that are male, and whether the relative had cancer in both breasts (bilateral breast cancer,) and a combination of two or more first or second degree relatives diagnosed with ovarian cancer, no matter what their age was when diagnosed.…

    • 553 Words
    • 3 Pages
    Satisfactory Essays
  • Better Essays

    Breast cancer is a common malignancy diagnosed in women. In the United States one in eight women who live to the age of 95 will be diagnosed with breast cancer. Even with the high rate of diagnosis, it remains the most treatable due to early screening and improved detection methods. Mammography is the precedent for screening and diagnostic procedures in the breast cancer field. Its enhancements through the years, together with higher resolution, faster, lower-dose screen-film combinations, have contributed to earlier cancer detection in women.…

    • 1667 Words
    • 7 Pages
    Better Essays
  • Better Essays

    These listed above are some ideas that were mentioned in this article. If you already have a pre disposition of getting breast cancer than you can try and not drink so much alcohol, watch your weight, and exercise. But doing all that and have a strong family history will not totally clean you of your chances of having breast cancer; it just helps to lower if possible your percentage of having…

    • 614 Words
    • 3 Pages
    Better Essays
  • Good Essays

    Anatomy Pictures

    • 598 Words
    • 3 Pages

    cancer is two to three times greater than an average person. But risk is still small, and a lot of the times, the gene will not even be found. Basically, anyone can develop mutated genes from the…

    • 598 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    If there are any serious imperfections in the gene code, then it is highly likely that a mutation has occurred to the BRCA1 gene, and the patient is informed as such (Healthwise: 2011). However, this highly invasive test can cause extreme anxiety and, if every medical practitioner notified relatives if cancer patients so that genetic testing could be conducted, many of the relatives of these cancer patients would suffer further anxiety, while additional financial strain would be placed on the already limited resources…

    • 2057 Words
    • 9 Pages
    Powerful Essays
  • Powerful Essays

    Ruth Chadwick, the author of “Drug Discovery Today: Therapeutic Strategies”, revealed her concerns for the personalized medicine movement, “The move towards personalized medicine may disadvantage some patients in some social contexts, by shifting the allocation of resources in the health care system. Risks also surround the increasing accumulation of health data that goes hand in hand with personalized medicine” (Chadwick 171). Chadwick refers to the collection of personal DNA test information, “accumulation of healthcare data” as a risk; however, with the increased informational knowledge brought in by personalized medicine testing, cancer or other incurable diseases could benefit from an increased database of information. The risks mentioned by Chadwick may elude to an ethical argument for the increased concerns as personalized medicine comes to mainstream healthcare. Ideally, the increase in genetic testing among individuals through the implementation of personalized medicine would bring in massive amounts of information regarding the precursors for diseases and cancer allowing medical attention to become more accurate.…

    • 1774 Words
    • 8 Pages
    Powerful Essays
  • Good Essays

    Genetic testing is being used in the medical field to decrease dangers in patients. The negative connotations brought by these examinations might be the reason a person, whom may have had great talents, will lower their capacity to excel. Insurance companies grant pensions and healthcare, consequently if a person were to be diagnosed even with a minimal chance of cancer by…

    • 478 Words
    • 2 Pages
    Good Essays
  • Good Essays

    From a patient’s perspective, people tend to see genetic information as more definitive, in the sense that 'you cannot change your genes' and that 'genes tell all about your future.’ Such genetic determinism is an oversimplification and does not take into account the nature of biologic pathways. From a provider’s perspective, genomics presents challenges with respect to ethical and professional responsibilities, including the appropriate use of genomic information in the health care setting. I believe that there should be an identification of provider education programs that increase use of appropriate screening, counseling and evidence-based genetic tests. By increasing the effectiveness of genomic testing, it will help dissolve the negative association and further increase the proportion of people who are willing to receive genetic…

    • 463 Words
    • 2 Pages
    Good Essays
  • Good Essays

    Genetic testing, aka DNA testing, allows doctors to check if there are any possibilities to inherit diseases, and can also be used to determine a person's ancestry or biological relationship between people. It is important to understand the background and implications behind genetic testing as testing may be able to identify the odds of have of having a child with a genetic disease, but it can also result in miscarriage. The test often cannot determine if the child will show symptoms of a disease, how severe the symptoms will be, or whether the disease will progress over time. Another thing to take into consideration is the absence of treatment strategies…

    • 714 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    When using genetic technology in personalized medicine is that some patients may receive incorrect information about their disease risk. This will bring up liability issue for them providing and prescribing the wrong preventive drug that may cause the individual to have severe to fatal side effects. The information can be falsely given but the patient has the burden of proof when it comes to filling a claim for negligence. This genetic testing that would lead to personalized medicine also causes the potential risk of stress on a patient when you put the thought into their heads that they may contract a certain disease that may be life threatening. There are many other drawbacks. The question of how accurate the tests are comes into play, being that there is no accuracy measurement in place for most. When given the results “Say you are tested for the potential for lung cancer, and learn that you might develop it someday. You decide not to smoke and you don’t develop it. But you can’t now know whether the test was right or wrong to begin with because you took steps not to develop it.”(Torrey, 2010) You also need someone who is trained in translating the results for you. Also your privacy is really not yours because you’re DNA can also be like your social and be kept, sold, and they even may us it however they see fit for their personal gain. The HIPPA laws don’t cover genetic testing so you’re not protected at all. The main drawback right now is that they aren’t effective enough in the early stages of the development. In the future with more test and better laws in place Genetic testing will make the personalized healthcare business…

    • 570 Words
    • 3 Pages
    Satisfactory Essays
  • Good Essays

    Chronic Diseases

    • 711 Words
    • 3 Pages

    Finding out that you have any type of cancer will change your life and wonder how and why it happens to them. Even after many years and billions of dollars of research, we still don't know exactly what causes cancer. But we do know how to identify people who are at higher risk of developing specific cancers. A well-known cancer that majority women get but also men can get as well is breast cancer. Breast cancer is a cancer that starts in the tissues of the breast. Everyone has a risk factor; a risk factor is anything that affects your chances of getting a particular disease. They are risk factors that you cannot change and those are: age, gender, family history of breast cancer, genes, and menstrual cycle.…

    • 711 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    What Is Breast Cancer

    • 4209 Words
    • 17 Pages

    Breast cancer is just one type of cancer. Cancerous cells are cells that grow without the normal system of controls placed upon them. Breast cancer develops from the mammary ducts 80% of the time. The other 20% of the time the cancer develops from the lobules of the breasts. While breast cancer may occur in men, this paper will primarily focus on breast cancer in women. Breast cancer is 100 times more likely to affect women as it is men. There are two forms of breast cancer, invasive cancer and carcinoma in situ. (Dimensions of Human Sexuality, Shriver, S. 2002)…

    • 4209 Words
    • 17 Pages
    Powerful Essays
  • Good Essays

    “Cancer is the leading cause of death worldwide and afflicts two of every three families.” (Zelman, M., Holdaway, P., Tompary, E., Raymond, J. & Mulvihill, M.L., 2010). Breast cancer is the most frequent diagnosed cancer in women. More than one million cases occur worldwide annually (Zelman, M., Holdaway, P., Tompary, E., Raymond, J. & Mulvihill, M.L., 2010). When it comes to breast cancer there are many areas that you should look at to understand, and be aware of. The areas are to know the cause and risk factors, prevention and detection, the effects on your health, and lastly your treatment options. We will cover each of these areas throughout this essay.…

    • 1496 Words
    • 6 Pages
    Good Essays

Related Topics