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Cervical Cancer |
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Cervical cancer is a disease in which malignant (cancer) cells form in the tissues of the cervix. The cervix is the lower, narrow end of the uterus (the hollow, pear-shaped organ where a fetus grows). The cervix leads from the uterus to the vagina (birth canal). Cervical cancer usually develops slowly over time. Before cancer appears in the cervix, the cells of the cervix go through changes known as dysplasia, in which cells that are not normal begin to appear in the cervical tissue. Later, cancer cells start to grow and spread more deeply into the cervix and to surrounding areas. Human papillomavirus (HPV) infection is the major risk factor for development of cervical cancer. There are now effective vaccines against certain types of HPV. Early cervical cancer may not cause noticeable signs or symptoms. Women should have yearly check-ups, including a Pap smear to check for abnormal cells in the cervix. The prognosis (chance of recovery) is better when the cancer is found early. These and other symptoms may be caused by cervical cancer. Other conditions may cause the same symptoms. A doctor should be consulted if any of the following problems occur:
To diagnose cervical cancer, the following procedures may be used:
All cancers are caused by dysfunctions of proteins involved in cell division, apoptosis, or DNA repair (see general characteristics). Dysfunctional proteins may arise from gene mutations or protein interaction with environments such as viral proteins. About 70% of cervical cancer patients are infected with HPV type 16 or 18. The genomes of HPV 16 and HPV 18 encode two proteins, E6 and E7, which can inactivate two crucial proteins involved in cell division: p53 and pRB (more info).
Reference: National Cancer Institute, USA.
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