Department of Dermatology, The School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Department of Dermatology, Columbia University, New York, New York, USA.
J Invest Dermatol. 2022 Dec;142(12):3253-3261.e4. doi: 10.1016/j.jid.2022.06.005. Epub 2022 Jul 1.
Combined BET inhibitor/histone deacetylase inhibitor treatment induces marked apoptosis of cutaneous T-cell lymphoma (CTCL) with minimal normal T-cell toxicity. At 96 hours when apoptosis was extensive, a majority of CTCL lines showed ≥2-fold suppression of T-cell survival factors (e.g., AKT1, BCL2 antiapoptotic factors, BIRC5, CD40, CD70, GADD45A, PRKCA, TNFRSF1B, ΔNp73) and ≥2-fold upregulation of proapoptotic factors and tumor suppressors (e.g., ATM, BAK, BIM, multiple caspases, FHIT, HIC1, MGMT, NOD1) (P < 0.05). The largest alterations were in TP73 isoform expression, resulting in increased TAp73/ΔNp73 ratios in CTCL lines and leukemic Sézary cells. Targeted ΔNp73 inhibition by small interfering RNA knockdown resulted in robust CTCL apoptosis comparable with that induced by BET inhibitor/histone deacetylase inhibitor with minimal normal T-cell toxicity. Chromatin immunoprecipitation analysis showed that BET inhibitor/histone deacetylase inhibitor treatment reduced RNA polymerase II binding to ΔNp73, MYC, and AKT1 while increasing its binding to TAp73. CTCL skin lesions expressed both TAp73 and ΔNp73 isoforms in situ. In aggregate, these findings implicate TAp73/ΔNp73 balance as a major factor governing CTCL survival, show that the expression of p73 isoforms can be altered by molecular biological and pharmaceutical means, show that p73 isoforms are expressed across the entire CTCL clinical spectrum, and identify the p73 pathway as a potential target for therapeutics.
联合 BET 抑制剂/组蛋白去乙酰化酶抑制剂治疗可显著诱导皮肤 T 细胞淋巴瘤 (CTCL) 的凋亡,而对正常 T 细胞的毒性最小。在凋亡广泛发生的 96 小时时,大多数 CTCL 系表现出 T 细胞存活因子(如 AKT1、BCL2 抗凋亡因子、BIRC5、CD40、CD70、GADD45A、PRKCA、TNFRSF1B、ΔNp73)的 2 倍以上抑制和促凋亡因子和肿瘤抑制因子(如 ATM、BAK、BIM、多种半胱天冬酶、FHIT、HIC1、MGMT、NOD1)的 2 倍以上上调(P < 0.05)。最大的改变是 TP73 异构体的表达,导致 CTCL 系和白血病性 Sézary 细胞中的 TAp73/ΔNp73 比值增加。通过小干扰 RNA 敲低靶向抑制 ΔNp73 可导致 CTCL 凋亡增强,与 BET 抑制剂/组蛋白去乙酰化酶抑制剂诱导的凋亡相当,而对正常 T 细胞的毒性最小。染色质免疫沉淀分析显示,BET 抑制剂/组蛋白去乙酰化酶抑制剂治疗可减少 RNA 聚合酶 II 与 ΔNp73、MYC 和 AKT1 的结合,同时增加其与 TAp73 的结合。CTCL 皮肤病变原位表达 TAp73 和 ΔNp73 异构体。总之,这些发现表明 TAp73/ΔNp73 平衡是决定 CTCL 存活的主要因素,表明 p73 异构体的表达可以通过分子生物学和药物手段改变,表明 p73 异构体在整个 CTCL 临床谱中表达,并确定 p73 途径为潜在的治疗靶点。