靶向BCL6和STAT3治疗三阴性乳腺癌:组合拳?

Sarah R Walker, D. Frank
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引用次数: 8

摘要

乳腺癌仍然是美国妇女癌症死亡的第二大原因。三阴性乳腺癌,即缺乏雌激素受体、孕激素受体和Her2的肿瘤,仅占确诊乳腺肿瘤的20-30%。然而,由于缺乏针对ER+或Her2+肿瘤的特异性靶向治疗,它们导致了许多乳腺癌死亡。为了开发针对三阴性乳腺癌的靶向治疗,可能需要抑制两个靶点。一个令人感兴趣的新靶点是转录调节剂BCL6,它最近被发现在乳腺癌中起重要作用[1-3]。BCL6被认为是一种转录抑制因子,它可以招募各种辅助抑制因子复合物来抑制其靶基因;然而,也发现了BCL6上调的基因[1,2],包括参与促进EMT[3]的Zeb1。虽然BCL6在阻止生发中心B细胞终末分化和促进弥漫性大B细胞淋巴瘤中的作用是众所周知的,但目前对BCL6在实体组织中的作用知之甚少。BCL6在约50%的乳腺肿瘤中扩增,并在大多数乳腺癌细胞系中表达,包括三阴性乳腺癌细胞系[1]。此外,BCL6表达与疾病进展和较差的总生存期[2]相关,靶向BCL6可导致乳腺癌细胞生长减少和活力丧失[1]。重要的是,三阴性乳腺癌细胞系对BCL6的抑制最为敏感。在正常乳腺中,BCL6已被证明可以阻止终末分化和泌乳,部分原因是BCL6与信号换能器和转录激活因子5 (STAT5)竞争调控靶基因[4]。STATs是潜伏在细胞质中的转录因子,通常通过Jak激酶被酪氨酸磷酸化激活。然后它们作为活性二聚体转移到细胞核并调节目标基因的转录。STAT家族共有7个成员,其中STAT1、STAT3、STAT5a、STAT5b 4个成员调控BCL6的表达。STAT1和STAT3上调BCL6表达,而STAT5 (5a和5b)下调BCL6表达[5]。所有四种stat都被证明在乳腺癌中起作用;然而,STAT3的激活与更具侵略性的类型有关。虽然STAT3激活可以发生在任何亚型乳腺癌[5]中,但STAT3激活主要局限于三阴性乳腺癌细胞系,STAT3信号传导已被证明对三阴性乳腺癌[6]的存活很重要。BCL6和STAT3都在三阴性乳腺癌中发挥关键作用,包括通过调节不同的靶基因促进生存和EMT。因此,针对这两个因素是否可以作为治疗三阴性乳腺癌的有效策略呢?用siRNA或拟肽i - bpi[7]抑制BCL6,同时用Jak激酶抑制剂TG101348或nifuroxazide抑制STAT3,可增强对三阴性乳腺癌细胞系[1]的杀伤。这些发现表明,同时针对两种致癌转录调节剂的靶向治疗可能是治疗三阴性乳腺癌的新途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting BCL6 and STAT3 in triple negative breast cancer: the one-two punch?
Breast cancer remains the second leading cause of cancer deaths in women in the United States. Triple negative breast cancer, tumors lacking estrogen receptor, progesterone receptor, and Her2, only comprise about 20–30% of breast tumors diagnosed. However, due to the lack of specific targeted therapy as exists for ER+ or Her2+ tumors, they account for many of the breast cancer deaths. To develop targeted therapy for triple negative breast cancer, inhibiting two targets may be necessary. One new target of interest is the transcriptional modulator BCL6 which has been recently identified as playing an important role in breast cancer [1–3]. BCL6 has been characterized as a transcriptional repressor that recruits various corepressor complexes to repress its target genes; however, genes have also been identified that are upregulated by BCL6 [1, 2], including Zeb1 which is involved in promoting EMT [3]. While the roles of BCL6 in preventing terminal differentiation of B cells in the germinal center and promoting diffuse large B cell lymphoma are well known, little is currently known about the roles of BCL6 in solid tissue. BCL6 is amplified in ∼50% of breast tumors and is expressed in most breast cancer cell lines, including triple negative breast cancer cell lines [1]. Furthermore, BCL6 expression is correlated with disease progression and poor overall survival [2], and targeting BCL6 results in reduced growth and loss of breast cancer cell viability [1]. Importantly, triple negative breast cancer cell lines were among the most sensitive to BCL6 inhibition. In the normal mammary gland, BCL6 has been shown to prevent terminal differentiation and milk production, in part due to competition with signal transducer and activator of transcription 5 (STAT5) for regulation of target genes [4]. STATs are latent transcription factors that remain in the cytoplasm until activated by tyrosine phosphorylation often via Jak kinases. They then translocate to the nucleus as an active dimer and modulate transcription of target genes. There are seven members of the STAT family and four members, STAT1, STAT3, STAT5a, and STAT5b regulate the expression of BCL6. While STAT1 and STAT3 upregulate BCL6 expression, STAT5 (5a and 5b) downregulates BCL6 expression [5]. All four STATs have been shown to play roles in breast cancer; however, STAT3 activation has been linked to more aggressive types. While STAT3 activation can occur in any subtype of breast cancer [5], STAT3 activation is restricted largely to triple negative breast cancer cell lines, and STAT3 signaling has been shown to be important for the survival of triple negative breast tumors [6]. Both BCL6 and STAT3 play critical roles in triple negative breast cancer, including promoting survival and EMT, through modulating largely distinct target genes. Thus, could targeting these two factors together be a useful strategy for specifically treating triple negative breast cancer? Inhibition of BCL6 by siRNA or the peptidomimetic RI-BPI [7] in conjunction with inhibition of STAT3 with the Jak kinase inhibitors TG101348 or nifuroxazide led to enhanced killing of triple negative breast cancer cell lines [1]. These findings suggest that targeted therapy directed simultaneously towards two oncogenic transcriptional modulators may be a new avenue for the treatment of triple negative breast cancer.
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