Causes Of Uterine Cancer

In the U.S. there are 35,000 women who are diagnosed with a new case of cancer of the uterus every year and in the same year 4,500 women die of the disease.

These statistics have not changed over the last decade. The peak age group for women who develop uterine cancer is age 55 to 60. Only about 5% of cases are reported in women below age 40 (data from Ref. 1 and 2). This table (data from Ref. 1, page 1195 and 1196) may need some explanation:

Until recently these factors were simply noted as an increased risk, but were not thought to be related to each other. Recent eicosanoid research, however, found the missing link (Ref. 3, page 144).

Factors associated with increased risk of uterine cancer:
obesityestrogen secreting ovarian tumor
late menopauseunopposed estrogen pills or injections
never had a babysyndrome of insulin resistance
polycystic ovaries hypertension
diabetes arthritis
hypothyroidismrare genetic syndromes (moderate risk)

 

It appears that the one of the culprits is a high insulin level, which changes the body chemistry. All of the conditions mentioned in the table are in some way related to this syndrome of insuline resistance or "syndrome X", how it was called in the 1980's and early 1990's. Now it has been renamed as "metabolic syndrome". It is the combination of obesity, polycystic ovary syndrome, diabetes, and hypertension. High insulin levels can cause many forms of arthritis due to "bad eicosanoids" (for further details see Ref. 3). As Dr. Sears, the inventor of the zone diet, stated the "bad eicosanoids that increase insulin secretion are the same ones that increase the likelihood of heart disease, cancer, and arthritis" (Ref. 3, page 144). A Swedish study (Ref.4) confirmed that there is a high risk of uterine cancer in patients with diabetes, hypertension and obesity.

"The 'bad eicosanoids' that increase insulin secretion are the same ones that increase the likelihood of heart disease, cancer, and arthritis" (Dr. Sears, Ref. 3, page 144).

Another culprit is unopposed estrogen exposure of the endometrial lining of the uterus leading to an increased risk of uterine cancer (late menopause, never had a baby, estrogen secreting tumor and unopposed estrogen as pills or injections). On the other hand, the birth control pill was shown to cut the risk for uterine cancer to about 70% to 80% compared to a woman who does not use hormone pills or injections. The reason is that estrogen production from the ovaries is blocked when outside hormones are given, even when women take modified estrogen or progesterone molecules as with synthetic hormone products. The same reasoning what is true for the BCP holds true for postmenopausal hormone replacement, which is usually known under "ERT" meaning "estrogen replacement therapy".

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For many years physicians paid attention mainly to estrogen, because its lack causes a postmenopausal woman get hot flushes and vaginal dryness. However, when reports of increased uterine cancer rates appeared in the medical literature, research was carried out, which showed that a birth-control pill like combination of small amounts of additional progestin (like Provera) with estrogen rendered the estrogen risk neutral or similar to the birth control pill. The physician still must watch the side-effects of too much progestin, which leads to clotting problems including strokes. This came out from the Women's Health Initiative (Ref. 13). As a result of these developemtns we now know that only bio-identical hormones should be given for hormone replacement (HRT) in the proper mix to reduce the risk for uterine cancer, breast cancer and colon cancer.

Finally there are some rarer cases of genetic traits in certain families where there is a moderate risk of increased uterine cancer rates. For more info on uterine cancer click on "uterine cancer".

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Disclaimer:

This outline is only a teaching aid to patients and should stimulate you to ask the right questions when seeing your doctor. However, the responsibility of treatment stays in the hands of your doctor and you.

References:

1. Cancer: Principles &Practice of Oncology.4th edition. Edited by Vincent T. DeVita, Jr. et al. Lippincott, Philadelphia,PA, 1993. Vol. 1. Chapter on gynecological tumors.

2. Cancer: Principles&Practice of Oncology. 5th edition, volume 1. Edited by Vincent T. DeVita, Jr. et al. Lippincott-Raven Publ., Philadelphia,PA, 1997. Chapter on gynecological tumors.

3. B. Sears: "The age-free zone". Regan Books, Harper Collins, 2000.

4. E Weiderpass et al. Cancer Causes Control 2000 Feb;11(2):185-192.

5. S Shibutani et al. Cancer Res 2001 May 15;61(10):3925-3931.

6. DB Fournier et al. Gynecol Oncol 2001 Jun;81(3):366-372.

7. DS McMeekin et al. Gynecol Oncol 2001 May;81(2):273-278.

8. LA Katz et al. Am J Obstet Gynecol 2001 May;184(6):1071-1073.

9. B Bonanni et al. Breast J 2000 Oct;6(5):317-323.

10. MG Jain et al. Eur J Epidemiol 2000;16(10):899-905.

11. Conn's Current Therapy 2004, 56th ed., Copyright © 2004 Elsevier

12. Ferri: Ferri's Clinical Advisor: Instant Diagnosis and Treatment, 2004 ed., Copyright © 2004 Mosby, Inc

13. Writing Group for the Women's Health Initiative Investigators: Risks and benefits of estrogen plus progestin in healthy postmenopausal women. Principal results from the Women's Health Initiative randomized controlled trial. JAMA 2002;288:321-333.

Last Modified: April 12, 2012