Key result
CaV1.3 showed reduced nuclear expression in neoplastic lesions, while cytoplasmic CaV1.1 and membrane CaV1.2 and CaV1.3 expression increased as lesions progressed to invasive carcinomas.
Why the study?
The role of L-type voltage-dependent Ca2+ channels in breast cancer development from non-obligate precursors had not been investigated.
Observational
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Background Intracellular Ca 2+ levels can modulate several cellular functions, including proliferation and other processes found altered in neoplastic cells. Helping to maintain Ca 2+ homeostasis, L-type voltage-dependent Ca 2+ channels had its expression identified in neoplasias, including breast cancer. Invasive breast carcinoma of no special type, the most common classification of breast cancer, has ductal hyperplasia and ductal carcinoma in situ as its possible non-obligate precursors. This channel’s role in breast cancer development from these precursors has not been investigated. Evaluate protein expression and subcellular localization of Ca V 1.1, Ca V 1.2, and Ca V 1.3 in mammary epithelium without alteration and neoplastic and non-neoplastic ductal proliferative lesions through immunohistochemistry was the aim of this investigation. Methods In the present study, Ca V 1.1, Ca V 1.2, and Ca V 1.3 protein expression was evaluated by immunohistochemistry in breast without alteration and in proliferative non-neoplastic and neoplastic ductal epithelial lesions of the human breast. Results It was observed that Ca V 1.3 presented a reduction in nuclear expression at neoplastic lesions, in addition to an increase in cytoplasmic Ca V 1.1 expression. The analyses of membrane immunostaining showed that Ca V 1.2 and Ca V 1.3 had an increase of expression as the lesions progressed in the stages leading to invasive carcinomas. Conclusions Changes in protein expression and subcellular localization of these channels during the progression stages indicate that they may be involved in neoplastic transformation.
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Aguiar et al. (2022) conducted an observational in Breast cancer. Immunohistochemistry for CaV1.1, CaV1.2, and CaV1.3 vs. Mammary epithelium without alteration was evaluated on Protein expression and subcellular localization of CaV1.1, CaV1.2, and CaV1.3. CaV1.3 showed reduced nuclear expression in neoplastic lesions, while cytoplasmic CaV1.1 and membrane CaV1.2 and CaV1.3 expression increased as lesions progressed to invasive carcinomas.
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