1982
DOI: 10.1016/s0140-6736(82)92260-7
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Colon Cancer and Sex

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1986
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Cited by 10 publications
(5 citation statements)
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“…It also demonstrated that such an oncofetal antigen may stimulate a mother during pregnancy and induce tumor resistance as shown by the increased resistance of multiparous rats to the challenge with RCA-1 tumor cells. In this connection, it is interesting to note that multiparous women ap pear less likely to develop colonic adenocarcinomas than are nulliparous women [17], The above results are in agreement with those by Sjogren [18], who showed that multiparous rats were more resistant to tumor induction by DMH than were virgin rats. He proposed that this resistance was induced by fetal cell-surface antigens shared by DMH-induced tu mors.…”
Section: Discussionsupporting
confidence: 88%
“…It also demonstrated that such an oncofetal antigen may stimulate a mother during pregnancy and induce tumor resistance as shown by the increased resistance of multiparous rats to the challenge with RCA-1 tumor cells. In this connection, it is interesting to note that multiparous women ap pear less likely to develop colonic adenocarcinomas than are nulliparous women [17], The above results are in agreement with those by Sjogren [18], who showed that multiparous rats were more resistant to tumor induction by DMH than were virgin rats. He proposed that this resistance was induced by fetal cell-surface antigens shared by DMH-induced tu mors.…”
Section: Discussionsupporting
confidence: 88%
“…STS is also present in colon carcinomas and many colorectal cancer cell lines [ 62 ], suggesting that this cancer, which is a major cause of cancer-related deaths in both men and women, might also be a potential target for STS inhibitor therapy [ 63 , 64 ]. In postmenopausal women, the reduction in oestrogen levels that occurs at menopause appears to be associated with a reduction in the risk of colorectal cancer [ 65 ]. Paradoxically, epidemiological data suggest a protective effect associated with the use of hormone replacement therapy [ 66 ].…”
Section: Steroid Sulphatase Expression and Activitymentioning
confidence: 99%
“…It has been inversely related to the risk of colorectal cancer (Platz and Giovannucci, 1999) and adenoma recurrence (Baron et al, 1999), but high intake of calcium has been positively associated with risk of other cancers, including prostate cancer (Chan and Giovannucci, 2001;Rodriguez et al, 2003). Calcium has been hypothesized to protect against colorectal cancer by binding secondary bile acids and ionized fatty acids in the colon to form insoluble soaps, thereby reducing their proliferative stimulus on colonic mucosa (Newmark et al, 1984;McMichael and Potter, 1985). Calcium may also directly reduce cellular proliferation in the colonic mucosa or cause terminal differentiation of cells (Lipkin and Newmark, 1985;Bostick, 1997;Lamprecht and Lipkin, 2001).…”
Section: Calciummentioning
confidence: 99%