Illinois Institute of Technology, Chicago, Illinois 60616, USA.
J Biol Chem. 2012 Oct 5;287(41):34722-9. doi: 10.1074/jbc.M112.374785. Epub 2012 Aug 21.
The pro-death Bcl-2 family protein and tumor suppressor Bax is frequently mutated in tumors with microsatellite instability (MSI). The mutation often results in a "Bax negative" phenotype and therefore is generally thought to be beneficial to the development of the tumor. Here, we report the identification of a novel Bax isoform, BaxΔ2, which is unique to microsatellite unstable tumors. BaxΔ2 is generated by a unique combination of a microsatellite deletion in Bax exon 3 and alternative splicing of Bax exon 2. Consistently, BaxΔ2 is only detected in MSI cell lines and primary tumors. BaxΔ2 is a potent cell death inducer but does not directly target mitochondria. In addition, BaxΔ2 sensitizes certain MSI tumor cells to a subset of chemotherapeutic agents, such as adriamycin. Thus, our data provide evidence that mutation and alternative splicing of tumor suppressors such as Bax are not always beneficial to tumor development but can be detrimental instead.
促死亡 Bcl-2 家族蛋白和肿瘤抑制因子 Bax 在具有微卫星不稳定性 (MSI) 的肿瘤中经常发生突变。这种突变通常导致“Bax 阴性”表型,因此通常被认为有利于肿瘤的发展。在这里,我们报告了一种新型 Bax 异构体 BaxΔ2 的鉴定,它是微卫星不稳定肿瘤所特有的。BaxΔ2 是由 Bax 外显子 3 中的微卫星缺失和 Bax 外显子 2 的选择性剪接的独特组合产生的。一致地,BaxΔ2 仅在 MSI 细胞系和原发性肿瘤中检测到。BaxΔ2 是一种有效的细胞死亡诱导剂,但不直接靶向线粒体。此外,BaxΔ2 使某些 MSI 肿瘤细胞对亚组化疗药物(如阿霉素)敏感。因此,我们的数据提供了证据,表明肿瘤抑制因子如 Bax 的突变和选择性剪接并不总是有利于肿瘤的发展,反而可能有害。