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KAT7 通过上调乳腺癌中的 PI3K/AKT 信号促进放射抵抗。

KAT7 promotes radioresistance through upregulating PI3K/AKT signaling in breast cancer.

机构信息

The First School of Clinical Medicine, Lanzhou University, Lanzhou, Gansu, 730000, P. R. China.

Department of Radiation Oncology, The First Hospital of Lanzhou University, Lanzhou University, Lanzhou, Gansu, 730000, P. R. China.

出版信息

J Radiat Res. 2023 Mar 23;64(2):448-456. doi: 10.1093/jrr/rrac107.

Abstract

Chromatin-modifying enzymes are commonly altered in cancers, but the molecular mechanism by which they regulate cancers remains poorly understood. Herein, we demonstrated that Lysine acetyltransferase 7 (KAT7) was upregulated in breast cancer. KAT7 expression negatively correlated with the survival of breast cancer patients, and KAT7 silencing suppressed breast cancer radioresistance in vitro. Mechanistically, KAT7 activated Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) transcription, leading to enhanced PI3K/AKT signaling and radioresistance. Overexpression of AKT or PIK3CA restored radioresistance suppression induced by KAT7 inhibition. Moreover, overexpression of KAT7, but not KAT7 acetyltransferase activity-deficient mutants promoted AKT phosphorylation at the Ser473 site, PIK3CA expression and radioresistance suppression due to KAT7 inhibition. In conclusion, KAT7 has huge prospects for clinical application as a new target for predicting radioresistance in breast cancer patients.

摘要

染色质修饰酶在癌症中通常发生改变,但它们调节癌症的分子机制仍知之甚少。在此,我们证明赖氨酸乙酰转移酶 7(KAT7)在乳腺癌中上调。KAT7 的表达与乳腺癌患者的生存呈负相关,KAT7 沉默抑制了体外乳腺癌的放射抵抗。在机制上,KAT7 激活了磷脂酰肌醇-4,5-二磷酸 3-激酶催化亚基 α(PIK3CA)转录,导致 PI3K/AKT 信号转导增强和放射抵抗。过表达 AKT 或 PIK3CA 可恢复 KAT7 抑制诱导的放射抵抗抑制。此外,过表达 KAT7(而非缺乏 KAT7 乙酰转移酶活性的突变体)促进了 AKT 在丝氨酸 473 位点的磷酸化、PIK3CA 的表达和由于 KAT7 抑制导致的放射抵抗抑制。总之,KAT7 作为预测乳腺癌患者放射抵抗的新靶点,具有巨大的临床应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05c7/10036104/fa026fd60a99/rrac107f1.jpg

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