Adenylate cyclase 9 expression level is associated with hormone receptor-positive breast cancer and predicts patient prognosis
Adenylate cyclase family members have recently received attention as novel therapeutic targets. However, the significance of adenylate cyclase 9 (ADCY9) in breast cancer has not been elucidated. Here, we evaluated expression in breast cancer (BC) cell lines, and polymerase chain reaction array analy...
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Veröffentlicht in: | Nagoya journal of medical science 2024-11, Vol.86 (4), p.665-682 |
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Sprache: | eng |
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Zusammenfassung: | Adenylate cyclase family members have recently received attention as novel therapeutic targets. However, the significance of adenylate cyclase 9 (ADCY9) in breast cancer has not been elucidated. Here, we evaluated
expression in breast cancer (BC) cell lines, and polymerase chain reaction array analysis was performed to determine the correlations between
expression levels and 84 tumor-associated genes. The association of
messenger RNA (mRNA) expression levels in clinical breast cancer specimens with patients' clinicopathological factors and prognosis was evaluated. The database of cancer cell line showed that estrogen receptor-positive and progesterone receptor-positive cells expressed higher
mRNA levels.
expression showed positive correlations with several oncogenes, such as
and
in the polymerase chain reaction array analysis. We defined the ratio of
mRNA expression levels in breast cancer and adjacent noncancerous tissues as the "C/N ratio". Among 149 patients with BC, estrogen receptor-positive and progesterone receptor-positive patients exhibited higher C/N ratios than estrogen receptor-negative and progesterone receptor-negative patients, respectively. Patients in the lowest C/N ratio quartile experienced shorter prognosis periods. The C/N ratio of
was found as an independent prognostic factor for disease-free survival. Thus,
expression is high in hormone receptor-positive breast cancer, and its low expression indicates a poor prognosis in patients with breast cancer. |
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ISSN: | 0027-7622 2186-3326 |
DOI: | 10.18999/nagjms.86.4.665 |