Department of Pharmacology, Chonnam National University Medical School, Gwangju, Republic of Korea.
College of Pharmacy, Sunchon National University, Suncheon, Republic of Korea.
Clin Transl Med. 2022 Jul;12(7):e871. doi: 10.1002/ctm2.871.
The stability of a protein, as well as its function and versatility, can be enhanced through oligomerization. KITENIN (KAI1 C-terminal interacting tetraspanin) is known to promote the malignant progression of colorectal cancer (CRC). How KITENIN maintains its structural integrity and stability are largely unknown, however. Here we investigated the mechanisms regulating the stability of KITENIN with the aim of developing therapeutics blocking its oncogenic functions. We found that KITENIN formed a homo-oligomeric complex and that the intracellular C-terminal domain (KITENIN-CTD) was needed for this oligomerization. Expression of the KITENIN-CTD alone interfered with the formation of the KITENIN homodimer, and the amino acid sequence from 463 to 471 within the KITENIN-CTD was the most effective. This sequence coupled with a cell-penetrating peptide was named a KITENIN dimerization-interfering peptide (KDIP). We next studied the mechanisms by which KDIP affected the stability of KITENIN. The KITENIN-interacting protein myosin-X (Myo10), which has oncogenic activity in several cancers, functioned as an effector to stabilize the KITENIN homodimer in the cis formation. Treatment with KDIP resulted in the disintegration of the homodimer via downregulation of Myo10, which led to increased binding of RACK1 to the exposed RACK1-interacting motif (463-471 aa), and subsequent autophagy-dependent degradation of KITENIN and reduced CRC cell invasion. Intravenous injection of KDIP significantly reduced the tumour burden in a syngeneic mouse tumour model and colorectal liver metastasis in an intrasplenic hepatic metastasis model. Collectively, our present results provide a new cancer therapeutic peptide for blocking colorectal liver metastasis, which acts by inducing the downregulation of Myo10 and specifically targeting the stability of the oncogenic KITENIN protein.
蛋白质的稳定性及其功能和多功能性可以通过寡聚化来增强。已知 KITENIN(KAI1 端尾相互作用四跨膜蛋白)可促进结直肠癌(CRC)的恶性进展。然而,KITENIN 如何保持其结构完整性和稳定性在很大程度上是未知的。在这里,我们研究了调节 KITENIN 稳定性的机制,旨在开发阻断其致癌功能的治疗方法。我们发现 KITENIN 形成同源寡聚复合物,并且细胞内 C 端结构域(KITENIN-CTD)是这种寡聚化所必需的。单独表达 KITENIN-CTD 会干扰 KITENIN 同源二聚体的形成,并且 KITENIN-CTD 内的 463 至 471 个氨基酸序列是最有效的。该序列与穿膜肽结合后被命名为 KITENIN 二聚化干扰肽(KDIP)。接下来,我们研究了 KDIP 影响 KITENIN 稳定性的机制。肌球蛋白-X(Myo10)是一种在几种癌症中具有致癌活性的 KITENIN 相互作用蛋白,作为效应子在顺式构象中稳定 KITENIN 同源二聚体。KDIP 的处理通过下调 Myo10 导致同源二聚体解体,导致 RACK1 与暴露的 RACK1 相互作用基序(463-471 aa)结合增加,随后自噬依赖性 KITENIN 降解和 CRC 细胞侵袭减少。KDIP 的静脉内注射在同基因小鼠肿瘤模型中显著降低了肿瘤负担,并在脾内肝转移模型中减少了结直肠癌肝转移。总之,我们的研究结果提供了一种新的用于阻断结直肠癌肝转移的癌症治疗肽,其通过诱导 Myo10 的下调并特异性靶向致癌性 KITENIN 蛋白的稳定性而起作用。