Prognostic significance of branched-chain amino acid transferase 1 and CD133 in triple-negative breast cancer.
トリプルネガティブ乳癌における分岐鎖アミノ酸転移酵素1とCD133の予後意義 (機械翻訳の邦題)
記録の確認項目
- 研究デザイン
- その他の原著論文
- 対象
- ヒト
- 出版年
- 2020
- 出典
- doi.org
- 抄録の表示
- 表示あり
- 出版状態
- 有効な記録
- 状態確認日
- 2026/08/17
- 収集日
- 2026/08/03
- 鮮度
- 確認期限内
- 確認段階
- 自動処理
- 記録状態
- 公開
日本語要約(機械生成)
トリプルネガティブ乳癌(TNBC)におけるBCAT1とCD133の発現と臨床病理学的特徴および予後との関連を検討した。291例のTNBC患者を対象に、組織マイクロアレイを用いて免疫組織化学染色で両マーカーの発現を評価した。追跡期間中央値は68.73ヶ月で、5年無病生存率は72.51%、全生存率は82.47%であった。BCAT1およびCD133の高発現はそれぞれ独立して無病生存期間と全生存期間の短縮と関連した。両マーカー高発現は36例(12.37%)に認められ、これらの患者は他の患者と比較して有意に短い無病生存期間と全生存期間を示した。BCAT1とCD133はTNBCの予後予測バイオマーカーとなり得る。
この要約は公開抄録のみを根拠にAIが機械的に生成したものです。正確な内容は原文を確認してください。
抄録
Background: Previous studies have shown that branched-chain amino acid transferase 1 (BCAT1) is associated with tumour progression in triple-negative breast cancer (TNBC). Furthermore, CD133 has emerged as a novel cancer stem cell marker for indicating tumour progression. However, the prognostic significance of these two markers remains to be verified. This study was conducted to investigate the correlation between BCAT1 and CD133 expression and clinicopathological features, as well as the prognosis of patients with TNBC.Methods: The study cohort included 291 patients with TNBC. Tissue microarrays were constructed for both cancer and normal tissues. The expression of BCAT1 and CD133 was detected by immunohistochemical staining, and the levels were evaluated using an H-scoring system. Cut-off points for BCAT1 and CD133 expression were determined using receiver operating characteristic curves.Results: The median follow-up time for the study participants was 68.73 months (range: 1.37-103.6 months). The 5-year disease-free survival (DFS) and overall survival (OS) rates of the 291 patients with TNBC were 72.51 and 82.47%, respectively. Higher levels of BCAT1 and CD133 expression independently indicated shorter DFS and OS. High levels of both BCAT1 and CD133 expression were detected in 36 (12.37%) patients, who had significantly shorter DFS and OS (both P < 0.001) compared to other patients.Conclusion: BCAT1 and CD133 can be considered as biomarkers with prognostic significance for TNBC.
MeSH
DOI 10.1186/s12885-020-07070-2
PMID 32571264
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