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Nectin-4:免疫球蛋白IgSF家族新靶點(diǎn),推動(dòng)多種腫瘤靶向藥物臨床轉(zhuǎn)化!

日期:2024-08-02 16:40:35

Nectin-4作為一種新發(fā)現(xiàn)的腫瘤標(biāo)志物,已在多種腫瘤患者的血清和組織中檢測(cè)到,并證實(shí)其表達(dá)增強(qiáng)了惡性腫瘤細(xì)胞的增殖、轉(zhuǎn)移和侵襲能力。Nectin-4對(duì)十多種癌癥具有顯著影響,早在2019年,靶向Nectin-4的抗體藥物偶聯(lián)物(ADCs)在癌癥治療領(lǐng)域取得了重要進(jìn)展,特別是Enfortumab Vedotin的問世并獲得FDA批準(zhǔn),用于治療局部晚期或轉(zhuǎn)移性尿路上皮癌,標(biāo)志著Nectin-4作為治療靶標(biāo)的重大突破。隨著科學(xué)研究的深入,Nectin-4作為惡性腫瘤生物標(biāo)志物的地位日益穩(wěn)固,同時(shí)展現(xiàn)出巨大的治療潛力。未來(lái),作為免疫球蛋白IgSF家族的一員,對(duì)Nectin-4與癌癥互動(dòng)機(jī)制的進(jìn)一步研究,將推動(dòng)更多創(chuàng)新藥物的研發(fā)!


1. 什么是Nectin-4?

1.1 Nectin-4的結(jié)構(gòu)

Nectin cell adhesion molecule 4(Nectin-4)是一種免疫球蛋白樣分子,屬于Nectin成員(還包括NECTIN-1、NECTIN-2NECTIN-3)。此外,Nectin-4與脊髓灰質(zhì)炎病毒受體(PVR/CD155)同源,也被稱作脊髓灰質(zhì)炎病毒受體相關(guān)蛋白PVRL4。Nectin-4作為免疫球蛋白超家族(IgSF)的一員,其分子量約為55.5 kDa,510個(gè)氨基酸構(gòu)建而成,展示出特有的三結(jié)構(gòu)域架構(gòu):蛋白的N端攜帶信號(hào)肽,引導(dǎo)其合成與定位;三個(gè)免疫球蛋白樣胞外結(jié)構(gòu)域,這些結(jié)構(gòu)域促進(jìn)細(xì)胞表面的相互識(shí)別與粘連;一個(gè)跨膜區(qū),將胞外結(jié)構(gòu)與胞內(nèi)環(huán)境連接;以及C端含afadin結(jié)合基序的胞內(nèi)結(jié)構(gòu)域,使Nectin-4能與afadin蛋白特異結(jié)合,促進(jìn)細(xì)胞間的粘附,影響細(xì)胞骨架組織及信號(hào)傳導(dǎo)(圖1[1-2]。

Nectin-4的結(jié)構(gòu)

圖1. Nectin-4的結(jié)構(gòu) [1]

1.2 Nectin-4的表達(dá)和功能

Nectin-4在細(xì)胞與細(xì)胞之間的粘附中扮演著關(guān)鍵角色。Nectin-4的三個(gè)免疫球蛋白(Ig)樣結(jié)構(gòu)域使其在多種生理過(guò)程中發(fā)揮作用,包括細(xì)胞粘附、信號(hào)轉(zhuǎn)導(dǎo)和細(xì)胞骨架的組織。與其它Nectins不同的是,Nectin-4在胚胎和胎盤組織中特異性地豐富表達(dá),而在成年組織中的表達(dá)則顯著下降。一項(xiàng)研究揭示Nectin4可能是TIGIT的新型配體,并證明針對(duì)Nectin4的特異性抗體可增強(qiáng)體外和體內(nèi)腫瘤細(xì)胞的殺傷。Nectin4還被鑒定為麻疹病毒屬成員的上皮受體,可能用于特異性靶向、感染和破壞表達(dá)Nectin-4/PVRL4的腫瘤。此外,越來(lái)越多的研究提示,NECTIN-4/Nectin-4的異常表達(dá)和活性可能促進(jìn)腫瘤細(xì)胞的生長(zhǎng)、擴(kuò)散和轉(zhuǎn)移,成為抗腫瘤治療的潛力靶標(biāo) [3-4]。


2. Nectin-4相關(guān)的信號(hào)機(jī)制

2.1 Nectin-4相關(guān)的細(xì)胞分子機(jī)制

Nectin-4是一種在腫瘤發(fā)展中扮演重要角色的蛋白質(zhì),它通過(guò)調(diào)控PI3K/AKT信號(hào)通路參與多種腫瘤進(jìn)程。在缺氧環(huán)境下,Nectin-4的細(xì)胞外部分脫落成為可溶性形式,與內(nèi)皮細(xì)胞上的整合素β4結(jié)合,激活Src、PI3K、Akt和eNOS等分子,促進(jìn)血管生成,此過(guò)程涉及NO的生成。例如,在乳腺癌中,Nectin-4與ERBB2協(xié)同作用,激活PI3K/AKT通路,促進(jìn)DNA合成;同時(shí),可溶性Nectin-4能通過(guò)PI3K/AKT軸激活Wnt/β-catenin信號(hào),促進(jìn)乳腺癌細(xì)胞增殖和轉(zhuǎn)移;Nectin-4還能激活PI3K/AKT/NF-κB通路,推動(dòng)骨肉瘤發(fā)展;并通過(guò)激活Rac1,促進(jìn)胃癌和膽囊癌的進(jìn)展(圖2[5]。

Nectin-4不僅作用于PI3K/AKT通路,還影響其他信號(hào)途徑。它與催乳素受體通過(guò)JAK2-STAT5a通路相互作用,對(duì)前列腺癌的生長(zhǎng)有重要作用。Nectin-4還能加強(qiáng)p95-ErbB2引發(fā)的JAK-STAT3信號(hào),并與之共同調(diào)控SOX2基因,促進(jìn)乳腺癌細(xì)胞的增殖。此外,Nectin-4通過(guò)調(diào)控CXCR4/CXCL12-LYVE-1軸,促進(jìn)腫瘤相關(guān)的淋巴管生成和淋巴轉(zhuǎn)移。一項(xiàng)研究還表明Nectin-4可以調(diào)節(jié)細(xì)胞間粘附、重塑肌動(dòng)蛋白細(xì)胞骨架、觸發(fā)上皮間充質(zhì)轉(zhuǎn)化EMT,并最終導(dǎo)致遠(yuǎn)處器官的腫瘤發(fā)展。這些發(fā)現(xiàn)揭示了Nectin-4在腫瘤細(xì)胞生物學(xué)中的廣泛作用,為癌癥治療提供了潛在的新靶點(diǎn)和策略 [6-8]。

Nectin-4通過(guò)調(diào)控PI3K/AKT信號(hào)通路參與多種腫瘤進(jìn)程

圖2. Nectin-4通過(guò)調(diào)控PI3K/AKT信號(hào)通路參與多種腫瘤進(jìn)程 [5]

2.2 Nectin-4相關(guān)的藥物研究機(jī)制

首個(gè)針對(duì)Nectin-4的ADC藥物(恩諾單抗,Enfortumab Vedotin-ejfv,以下簡(jiǎn)稱EV)已獲批用于治療尿路上皮癌。研究表明,EV是由蛋白酶依賴性的連接子綁定微管相關(guān)抑制劑(MMAE)與抗Nectin-4單克隆抗體(AGS-22M6)成的復(fù)合物。當(dāng)EV與癌細(xì)胞表面的Nectin-4蛋白結(jié)合時(shí),觸發(fā)內(nèi)吞作用,使得EV和Nectin-4形成的復(fù)合物進(jìn)入細(xì)胞內(nèi)部。進(jìn)入細(xì)胞后,不同的酶對(duì)EV復(fù)合物進(jìn)行部分水解。最終,EV被運(yùn)送到溶酶體,在溶酶體內(nèi)的酸性環(huán)境下被完全分解,從而釋放MMAE。MMAE阻止微管聚合,進(jìn)而分裂受到抑制,導(dǎo)致細(xì)胞凋亡。在臨床前研究中,EV顯著抑制了人膀胱癌、乳腺癌、肺癌和胰腺癌小鼠異種移植模型中的腫瘤生長(zhǎng)。這些研究結(jié)果,進(jìn)一步推動(dòng)了靶向Nectin-4的藥物在臨床研究中的轉(zhuǎn)化(圖3[5]。

靶向Nectin-4的藥物抑制腫瘤細(xì)胞的過(guò)程

圖3. 靶向Nectin-4的藥物抑制腫瘤細(xì)胞的過(guò)程 [5]


3. Nectin-4和疾病相關(guān)的研究

近年來(lái)Nectin-4因其在多種癌癥類型中異常過(guò)表達(dá)而受到關(guān)注,包括甲狀腺癌、食管癌、胃癌、膽囊癌、乳腺癌、皮膚癌、結(jié)直腸癌等,并與惡性腫瘤的診斷、治療、預(yù)后等顯著相關(guān)。正如前面提到的,靶向Nectin-4的ADC已被FDA批準(zhǔn)用于治療局部晚期或轉(zhuǎn)移性尿路上皮癌。鑒于其在癌癥中的作用,Nectin-4不僅成為診斷和預(yù)后的生物標(biāo)志物,也成為極具前景的腫瘤研究靶點(diǎn) [9]!

在消化系統(tǒng)癌癥中,以結(jié)直腸癌為例,Nectin-4不僅作為關(guān)鍵的生物標(biāo)志物,還通過(guò)與整合素β1的相互作用,促進(jìn)血管生成,對(duì)患者預(yù)后產(chǎn)生負(fù)面影響,并與對(duì)5-氟尿嘧啶(5-FU)的耐藥性相關(guān)。研究發(fā)現(xiàn),通過(guò)基因沉默技術(shù)下調(diào)Nectin-4的表達(dá),展示出治療結(jié)直腸癌的可能性 [10]。在食道癌中,Nectin-4的高表達(dá)與較短的患者生存期相關(guān),同時(shí)在細(xì)胞層面增強(qiáng)了食道癌細(xì)胞的活力和遷移能力 [11]。對(duì)于胃癌,Nectin-4的表達(dá)水平與不同的TNM分期緊密相關(guān) [12]。而在膽囊癌中,Nectin-4通過(guò)同一信號(hào)通路介導(dǎo)Rac1的激活,促進(jìn)腫瘤的生長(zhǎng)、增殖和轉(zhuǎn)移 [13]。

在生殖系統(tǒng)癌癥中,Nectin-4同樣扮演著重要角色。宮頸癌中,Nectin-4可能參與轉(zhuǎn)移性腫瘤的5-FU耐藥機(jī)制,其特定結(jié)構(gòu)域影響血管生成和DNA修復(fù)過(guò)程 [14]。在卵巢癌中,Nectin-4的高表達(dá)與疾病的發(fā)生、發(fā)展及球狀體形成密切相關(guān),進(jìn)而影響化療的效果 [15]。在呼吸系統(tǒng)腫瘤,如肺癌中,Nectin-4濃度的升高與生存期縮短、腫瘤侵襲性和易轉(zhuǎn)移性增加相關(guān),表明其在肺癌早期診斷中的潛在價(jià)值 [16]

泌尿系統(tǒng)腫瘤,尤其是尿路上皮癌,Nectin-4的高表達(dá)與不良預(yù)后因素如較高的癌癥死亡率、淋巴血管浸潤(rùn)和高級(jí)別腫瘤緊密相關(guān) [17]。Nectin-4還與多種其他癌癥類型有直接聯(lián)系,比如乳腺癌 [18]、肝癌 [19]、頭頸部癌 [20]、甲狀腺癌 [20]、黑色素瘤 [22]和皮膚鱗狀細(xì)胞癌 [23]。它在乳腺癌中可作為血清標(biāo)記物,在皮膚鱗狀細(xì)胞癌中作為生物標(biāo)志物,以及在黑色素瘤中與AKT/PI3K信號(hào)通路的調(diào)控密切相關(guān),這些發(fā)現(xiàn)共同強(qiáng)調(diào)了Nectin-4在癌癥研究和治療策略制定中的核心地位。


4. Nectin-4的臨床研究前景

目前,針對(duì)Nectin-4這一靶點(diǎn)的藥物研發(fā)中,只有Padcev(Enfortumab Vedotin)獲得FDA批準(zhǔn)上市,用于治療局部晚期或轉(zhuǎn)移性尿路上皮癌。Padcev的成功上市證明了NECTIN-4作為藥物靶點(diǎn)的可行性及其潛在的臨床價(jià)值。目前,Nectin-4不僅在尿路上皮癌中顯示出重要的治療潛力,而且在多種其他癌癥類型中也被認(rèn)為具有重要的臨床意義。令人期待的是,已有越來(lái)越多的研藥物正向臨床前和臨床1期階段邁進(jìn),這表明NECTIN-4靶點(diǎn)藥物研發(fā)活動(dòng)較為活躍。為促進(jìn)更多NECTIN-4靶向藥物成功上市,需要進(jìn)一步增加研發(fā)投入,優(yōu)化研發(fā)流程,提高成功率。大型制藥公司如Merck & Co., Inc.通常專注于臨床后期開發(fā),而小型及中型生物技術(shù)公司如BioAtla, Inc.和Elpis Biopharmaceuticals Corp.更多地參與早期臨床前研究。未來(lái),隨著更多臨床試驗(yàn)的展開和深入,預(yù)計(jì)將有更多基于Nectin-4的靶向藥物進(jìn)入臨床2/3期試驗(yàn),這將加速藥物的開發(fā)和上市進(jìn)程。

產(chǎn)品力薦

為鼎力協(xié)助各藥企針對(duì)Nectin-4在消化系統(tǒng)癌癥、生殖系統(tǒng)癌癥和泌尿系統(tǒng)腫瘤等在臨床中的研究,華美CUSABIO推出Nectin-4活性蛋白產(chǎn)品(Code: CSB-MP822274HU),助力您在對(duì)Nectin-4機(jī)制方面的研究或其潛在臨床價(jià)值的探索。

華美CUSABIO蛋白Nectin-4

Recombinant Human Nectin-4 (NECTIN4), partial (Active) Code: CSB-MP822274HU

Purity≥ 95% by SDS
CSB-MP822274HU-B Purity Verified

Purity was greater than 95% as determined by SDS-PAGE.

Activity Verified by a Functional ELISA
CSB-MP822274HU Activity Verified

Immobilized NECTIN4 at 2 μg/ml can bind anti-NECTIN4 antibody (CSB-RA822274A0HU) (enfortumab vedotin-like). The EC50 is 0.6029-0.7837 ng/mL.


參考文獻(xiàn):

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