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Bladder cancer
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Bladder cancer

Reviewed January 2007

What is bladder cancer?

Bladder cancer is a disease in which certain cells in the bladder become abnormal and multiply without control or order. The bladder is a hollow, muscular organ in the lower abdomen that stores urine until it is ready to be excreted from the body. The most common type of bladder cancer begins in cells lining the inside of the bladder and is called transitional cell carcinoma (TCC).

Bladder cancer may cause blood in the urine, pain during urination, frequent urination, or the feeling that one needs to urinate without results. These signs and symptoms are not specific to bladder cancer, however. They also can be caused by noncancerous conditions such as infections.

How common is bladder cancer?

In the United States, bladder cancer is the fourth most common type of cancer in men and the ninth most common cancer in women. About 45,000 men and 17,000 women are diagnosed with bladder cancer each year.

What are the genetic changes related to bladder cancer?

Bladder cancer is related to chromosome 9.

The FGFR3, HRAS, RB1, TP53, and TSC1 genes are associated with bladder cancer.

As with most cancers, the exact causes of bladder cancer are not known; however, many risk factors are associated with this disease. Many of the major risk factors are environmental, such as smoking and exposure to certain industrial chemicals. Studies suggest that chronic bladder inflammation, a parasitic infection called schistosomiasis, and some medications used to treat cancer are other environmental risk factors associated with bladder cancer.

Genetic factors are also likely to play an important role in determining bladder cancer risk. Researchers have studied the effects of mutations in several genes, including FGFR3, RB1, HRAS, TP53, and TSC1, on the formation and growth of bladder tumors. Each of these genes plays a critical role in regulating cell division by preventing cells from dividing too rapidly or in an uncontrolled way. Alterations in these genes may help explain why some bladder cancers grow and spread more rapidly than others.

Deletions of part or all of chromosome 9 are common events in bladder tumors. Researchers believe that several genes that control cell growth and division are probably located on chromosome 9. They are working to determine whether a loss of these genes plays a role in the development and progression of bladder cancer.

Most of the genetic changes associated with bladder cancer develop in bladder tissue during a person's lifetime, rather than being inherited from a parent. Some people, however, appear to inherit a reduced ability to break down certain chemicals, which makes them more sensitive to the cancer-causing effects of tobacco smoke and industrial chemicals.

Read more about the FGFR3, HRAS, RB1, TP53, and TSC1 genes and chromosome 9.

Can bladder cancer be inherited?

Bladder cancer is typically not inherited. Most often, tumors result from genetic mutations that occur in bladder cells during a person's lifetime. These noninherited genetic changes are called somatic mutations.

Where can I find information about treatment for bladder cancer?

These resources address the management of bladder cancer and may include treatment providers.

You might also find information on treatment of bladder cancer in Educational resources and Patient support.

Where can I find additional information about bladder cancer?

You may find the following resources about bladder cancer helpful. These materials are written for the general public.

You may also be interested in these resources, which are designed for healthcare professionals and researchers.

What other names do people use for bladder cancer?

  • Cancer of the bladder
  • Malignant tumor of urinary bladder
  • Urinary bladder cancer

What if I still have specific questions about bladder cancer?

Where can I find general information about genetic conditions?

What glossary definitions help with understanding bladder cancer?

cancer ; carcinoma ; cell ; cell division ; chromosome ; chronic ; deletion ; gene ; infection ; inflammation ; mutation ; neoplasms ; progression ; risk factors ; sign ; somatic mutation ; symptom ; tissue ; transitional cell carcinoma ; tumor

You may find definitions for these and many other terms in the Genetics Home Reference Glossary.

References (12 links)


The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? in the Handbook.

Reviewed: January 2007
Published: January 23, 2009