Sex differences of β-carotene effects in azoxymethane/dextran sulfate sodium-induced early colorectal cancer mice
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BACKGROUND/OBJECTIVES: Colorectal cancer (CRC) is a malignancy that occurs in the colon or rectum and ranks as the second leading cause of cancer-related fatalities globally. Numerous epidemiological studies have revealed a distinct difference in CRC between sexes. Specifically, a lower incidence rate and delayed onset in females than in males. β-Carotene (BC), a provitamin A carotenoid, elicits antioxidant effects; however, the potential sex- specific differences in its anti-colon cancer effect are unknown. This study aims to compare the effect of BC on inflammation between sexes in azoxymethane/dextran sulfate sodium (AOM/DSS)-induced early CRC. MATERIALS/METHODS: The AOM/DSS mouse model was established. In early CRC, systemic changes were assessed using the disease activity index (DAI), serum proinflammatory cytokine levels, estradiol, and retinol concentrations. Local changes were evaluated using colon length, tumor counts, proinflammatory cytokines, and estrogen receptor (ER) α expression in the colon. RESULTS: In early CRC-induced systemic changes, females had higher DAI scores and lower serum estradiol levels than males. DAI scores were decreased in both sexes, however, serum cytokine levels were reduced by BC supplementation only in females. In the early CRC model, the systemic disease activity in females was higher than that in males. Serum retinol concentrations decreased to a greater extent in female AOM/DSS-induced CRC mice than in their male counterparts. In terms of local changes, the colon was shorter and the ERα expression was increased in females. CONCLUSION: In early CRC, higher disease activity and specific changes, such as increased DAI scores and reduced serum estradiol in females than in males. BC supplementation could effectively reduce DAI scores and systemic inflammation in both sexes. Notably, serum cytokine levels decreased only in females.
Abstract
BACKGROUND/OBJECTIVES: Colorectal cancer (CRC) is a malignancy that occurs in the colon or rectum and ranks as the second leading cause of cancer-related fatalities globally. Numerous epidemiological studies have revealed a distinct difference in CRC between sexes. Specifically, a lower incidence rate and delayed onset in females than in males. β-Carotene (BC), a provitamin A carotenoid, elicits antioxidant effects; however, the potential sex- specific differences in its anti-colon cancer effect are unknown. This study aims to compare the effect of BC on inflammation between sexes in azoxymethane/dextran sulfate sodium (AOM/DSS)-induced early CRC. MATERIALS/METHODS: The AOM/DSS mouse model was established. In early CRC, systemic changes were assessed using the disease activity index (DAI), serum proinflammatory cytokine levels, estradiol, and retinol concentrations. Local changes were evaluated using colon length, tumor counts, proinflammatory cytokines, and estrogen receptor (ER) α expression in the colon. RESULTS: In early CRC-induced systemic changes, females had higher DAI scores and lower serum estradiol levels than males. DAI scores were decreased in both sexes, however, serum cytokine levels were reduced by BC supplementation only in females. In the early CRC model, the systemic disease activity in females was higher than that in males. Serum retinol concentrations decreased to a greater extent in female AOM/DSS-induced CRC mice than in their male counterparts. In terms of local changes, the colon was shorter and the ERα expression was increased in females. CONCLUSION: In early CRC, higher disease activity and specific changes, such as increased DAI scores and reduced serum estradiol in females than in males. BC supplementation could effectively reduce DAI scores and systemic inflammation in both sexes. Notably, serum cytokine levels decreased only in females.