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主页蛋白表达表皮生长因子受体 (EGFR) 信号传导

表皮生长因子受体 (EGFR) 信号传导

背景

表皮生长因子受体 (Epidermal growth factor receptor,EGFR) 是受体酪氨酸激酶家族 (receptor tyrosine kinase family,RTK) 中第一个被发现的原型成员。它被细胞外环境中的各种配体激活并传递细胞响应以介导各种细胞活动,包括细胞增殖、细胞存活、生长和发育。EGFR 在许多器官中有表达,异常表达与多种癌症有关。本文重点介绍了 EGFR 通路的各种信号成分及其信号转导通路。

表皮生长因子受体 (EGFR) 和配体

ErbB 家族由四种受体组成,包括 EGFR (ErbB-1/HER1)、ErbB-2 (Neu,HER2)、ErbB-3 (HER3) 和 ErbB-4 (HER4)。该受体酪氨酸激酶家族 (RTK) 具有胞外配体结合结构域、疏水跨膜结构域和胞质酪氨酸激酶结构域(表1)。ErbB 受体被 EGF-家族的生长因子激活,其特征在于赋予结合特异性的三个二硫键。其他结构基序包括免疫球蛋白样结构域,肝素结合位点和糖基化位点1,2。 

表1EGFR 受体和配体

受体激活

受体激活是由细胞膜上的一系列事件触发的。

  • 配体结合 每个配体与同源 ErbB 受体的胞外结构域结合
  • 受体二聚化  配体结合诱导形成受体同源或异源二聚体3
  • 激酶结构域的激活  羧基末端尾部关键酪氨酸残基的自磷酸化激活受体,并作为与 Src 同源 2 (SH2) 和磷酸酪氨酸结合域 (PTB) 蛋白的停靠位点,触发细胞信号传导3,4。 
egfr信号传导

图 1.EGFR信号传导

EGFR信号传导

Ras/Raf 信号级联

受体:  任何两种 ErbB 受体的二聚化

关键功能:关键功能: 细胞存活和细胞增殖5

受体激活后,Grb2 和 Sos 形成的复合物直接或通过衔接蛋白 Shc 结合到受体上的特定酪氨酸残基上6,7这导致 Sos 的构象变化,从而募集和激活 Ras-GDP。Ras-GDP 激活 Raf-1,后者进一步激活通过丝裂原活化蛋白激酶 (MAPK) 介导的细胞外调节激酶 1 和 2(ERK1 和 ERK2)8,9。活化的激酶最终进入细胞核,磷酸化特定的转录因子如 Elk1 和 C-myc 以诱导细胞增殖。

磷脂酰肌醇 3-激酶/Akt 信号级联反应

受体:  ErbB2 与 ErbB4 或 ErbB3 的二聚化

关键功能:  细胞生长、凋亡抵抗、细胞侵袭和迁移10

磷脂酰肌醇由 p85 和 p110 亚单位组成,这些亚单位与 ErbB 受体对接产生次级信使磷脂酰肌醇 3,4,5-三磷酸,后者进一步激活丝氨酸/苏氨酸激酶 AKT。激活后,AKT 磷酸化 mTOR 和随后介导蛋白质合成的 S6K10

信号转导和转录激活因子 (STAT) 途径

受体:ErbB

关键功能:  肿瘤进展、肿瘤发生和血管生成11

STAT 蛋白通过 Src 同源 2 个结构域与 ErbB 受体的磷酸酪氨酸残基对接,并在二聚化上向上,转位进入细胞核,促进特定靶基因如 Myc、Nos2、p21 和细胞因子的表达12

磷脂酶 Cγ 信号

受体:ErbB1

关键功能:调节离子通道、细胞迁移、钙介导的信号传导13

磷脂酶 Cγ 与 ErbB1 相互作用,水解磷脂酰肌醇 4,5-二磷酸 (PIP2) 生成肌醇 1,3,5-三磷酸 (IP3) 和 1,2 二酰甘油 (DAG)。IP3 增加细胞内钙水平,DAG 介导蛋白激酶 C (PKC) 的激活13。  激活的 PKC 依次激活 MAPK 和 c-Jun NH2-末端激酶14

Nck/PAK 信号级联

受体:ErbB1

关键功能:细胞存活和细胞迁移15

Nck 是一种含有 SH2 结构域的衔接蛋白,与 EGF 受体结合并触发下游信号。Nck 通过 SH3 结构域激活 PAK1(p21/CDC42/Rac1 激活的激酶-1)结合。激活的 PAK1 依次激活 MEKK1(MAP/ERK 激酶激酶-1)和 MKK4/7(MAP 激酶激酶-4/7)介导的 JNKs(c-Jun 激酶)。JNK 易位至细胞核并磷酸化转录因子如 c-Fos 和 c-Jun16

Cbl 介导的内吞作用

受体:ErbB1

关键功能:内吞作用

配体结合后,Cbl 是通过 SH2 结构域或通过 GRB2 衔接蛋白与 EGF 受体结合并触发受体溶酶体降解的底物17

EGFR 易位至细胞核

EGF 受体具有逃避溶酶体降解并转位进入细胞核以介导生物学功能的能力。在细胞核中,这些受体促进细胞存活基因如Cyclin D1基因的转录,也作为 STAT 和 E2F1 转录因子的辅助因子18。EGFR 的核定位通过赋予对抗癌单克隆抗体的生长抑制作用的抗性影响疾病的严重程度19

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发育与疾病中的 EGFR

EGF 受体 及其配体对各器官发育有重要意义;EGFR 敲除模型显示胚胎致死性和有缺陷的组织/器官。然而,ErbB 配体的突变不显示任何致死表型,因为其他配体的互补途径补偿了突变的 ErbB 配体的废除信号。20-25EGFR 在许多疾病中有异常激活或表达。具体而言,它们在癌症进展中的作用已得到很好的研究(表 2)。 

表2人类疾病中 EGFR 受体的遗传改变

结论

EGFR 信号在发育中具有多效性功能,调节多种生理功能。EGF 受体的异常表达已经越来越多地涉及各种疾病。还需要更多的研究来明确揭示 EGFR 信号在脑、心脏、皮肤、肾脏、乳腺和肺等多种器官发育中的作用。寻找具有高效、持续的药物活性和较少交叉反应性以对抗抗药性癌症的新型药物仍是当前的热点研究领域。

1.
Arteaga C, Engelman J. 2014. ERBB Receptors: From Oncogene Discovery to Basic Science to Mechanism-Based Cancer Therapeutics. Cancer Cell. 25(3):282-303. https://doi.org/10.1016/j.ccr.2014.02.025
2.
Kovacs E, Zorn JA, Huang Y, Barros T, Kuriyan J. 2015. A Structural Perspective on the Regulation of the Epidermal Growth Factor Receptor. Annu. Rev. Biochem.. 84(1):739-764. https://doi.org/10.1146/annurev-biochem-060614-034402
3.
Capuani F, Conte A, Argenzio E, Marchetti L, Priami C, Polo S, Di Fiore PP, Sigismund S, Ciliberto A. 2015. Quantitative analysis reveals how EGFR activation and downregulation are coupled in normal but not in cancer cells. Nat Commun. 6(1): https://doi.org/10.1038/ncomms8999
4.
Zhang X, Gureasko J, Shen K, Cole PA, Kuriyan J. 2006. An Allosteric Mechanism for Activation of the Kinase Domain of Epidermal Growth Factor Receptor. Cell. 125(6):1137-1149. https://doi.org/10.1016/j.cell.2006.05.013
5.
Gaestel M. 2006. MAPKAP kinases ? MKs ? two's company, three's a crowd. Nat Rev Mol Cell Biol. 7(2):120-130. https://doi.org/10.1038/nrm1834
6.
Lowenstein E, Daly R, Batzer A, Li W, Margolis B, Lammers R, Ullrich A, Skolnik E, Bar-Sagi D, Schlessinger J. 1992. The SH2 and SH3 domain-containing protein GRB2 links receptor tyrosine kinases to ras signaling. Cell. 70(3):431-442. https://doi.org/10.1016/0092-8674(92)90167-b
7.
Batzer AG, Rotin D, Ureña JM, Skolnik EY, Schlessinger J. 1994. Hierarchy of binding sites for Grb2 and Shc on the epidermal growth factor receptor.. Mol. Cell. Biol.. 14(8):5192-5201. https://doi.org/10.1128/mcb.14.8.5192
8.
B H, S I R, J D. 1994. Interaction of Ras and Raf in intact mammalian cells upon extracellular stimulation. J Biol Chem. 269(6):3913-6.
9.
Liebmann C. 2001. Regulation of MAP kinase activity by peptide receptor signalling pathway: Paradigms of multiplicity. Cellular Signalling. 13(11):777-785. https://doi.org/10.1016/s0898-6568(01)00192-9
10.
Vivanco I, Sawyers CL. 2002. The phosphatidylinositol 3-Kinase?AKT pathway in human cancer. Nat Rev Cancer. 2(7):489-501. https://doi.org/10.1038/nrc839
11.
Niu G, Wright KL, Huang M, Song L, Haura E, Turkson J, Zhang S, Wang T, Sinibaldi D, Coppola D, et al. 2002. Constitutive Stat3 activity up-regulates VEGF expression and tumor angiogenesis. Oncogene. 21(13):2000-2008. https://doi.org/10.1038/sj.onc.1205260
12.
Bromberg J. 2002. Stat proteins and oncogenesis. J. Clin. Invest.. 109(9):1139-1142. https://doi.org/10.1172/jci0215617
13.
Patterson RL, van Rossum DB, Nikolaidis N, Gill DL, Snyder SH. 2005. Phospholipase C-?: diverse roles in receptor-mediated calcium signaling. Trends in Biochemical Sciences. 30(12):688-697. https://doi.org/10.1016/j.tibs.2005.10.005
14.
Scho?nwasser DC, Marais RM, Marshall CJ, Parker PJ. 1998. Activation of the Mitogen-Activated Protein Kinase/Extracellular Signal-Regulated Kinase Pathway by Conventional, Novel, and Atypical Protein Kinase C Isotypes. Mol. Cell. Biol.. 18(2):790-798. https://doi.org/10.1128/mcb.18.2.790
15.
Ye DZ, Field J. 2012. PAK signaling in cancer. Cellular Logistics. 2(2):105-116. https://doi.org/10.4161/cl.21882
16.
Tomar A, Schlaepfer DD. 2010. A PAK-Activated Linker for EGFR and FAK. Developmental Cell. 18(2):170-172. https://doi.org/10.1016/j.devcel.2010.01.013
17.
Yu P, Fan Y, Qu X, Zhang J, Song N, Liu J, Liu Y. 2016. Cbl-b regulates the sensitivity of cetuximab through ubiquitin-proteasome system in human gastric cancer cells. J Buon. 21(4):867-873.
18.
Lo H, Hsu S, Ali-Seyed M, Gunduz M, Xia W, Wei Y, Bartholomeusz G, Shih J, Hung M. 2005. Nuclear interaction of EGFR and STAT3 in the activation of the iNOS/NO pathway. Cancer Cell. 7(6):575-589. https://doi.org/10.1016/j.ccr.2005.05.007
19.
Lo H, Xia W, Wei Y, MA, Huang S, Hung M. 2005. Novel prognostic value of nuclear epidermal growth factor receptor in breast cancer. Cancer Res. 65(1):338-48.
20.
Miettinen PJ, Berger JE, Meneses J, Phung Y, Pedersen RA, Werb Z, Derynck R. 1995. Epithelial immaturity and multiorgan failure in mice lacking epidermal growth factor receptor. Nature. 376(6538):337-341. https://doi.org/10.1038/376337a0
21.
Sibilia M, Wagner E. 1995. Strain-dependent epithelial defects in mice lacking the EGF receptor. Science. 269(5221):234-238. https://doi.org/10.1126/science.7618085
22.
Park S, Miller R, Krane I, Vartanian T. 2001. The erbB2 gene is required for the development of terminally differentiated spinal cord oligodendrocytes. 154(6):1245-1258. https://doi.org/10.1083/jcb.200104025
23.
Leu M. 2003. Erbb2 regulates neuromuscular synapse formation and is essential for muscle spindle development. 130(11):2291-2301. https://doi.org/10.1242/dev.00447
24.
S L E, K S O, N G, L L, G F, M B, L H L, M W M. 1997. ErbB3 is required for normal cerebellar and cardiac development: a comparison with ErbB2-and heregulin-deficient mice. Development. 124(24):4999-5011.
25.
Golub MS, Germann SL, Lloyd K. 2004. Behavioral characteristics of a nervous system-specific erbB4 knock-out mouse. Behavioural Brain Research. 153(1):159-170. https://doi.org/10.1016/j.bbr.2003.11.010
26.
Maheswaran S, Sequist LV, Nagrath S, Ulkus L, Brannigan B, Collura CV, Inserra E, Diederichs S, Iafrate AJ, Bell DW, et al. 2008. Detection of Mutations inEGFRin Circulating Lung-Cancer Cells. N Engl J Med. 359(4):366-377. https://doi.org/10.1056/nejmoa0800668
27.
Montagut C, Dalmases A, Bellosillo B, Crespo M, Pairet S, Iglesias M, Salido M, Gallen M, Marsters S, Tsai SP, et al. 2012. Identification of a mutation in the extracellular domain of the Epidermal Growth Factor Receptor conferring cetuximab resistance in colorectal cancer. Nat Med. 18(2):221-223. https://doi.org/10.1038/nm.2609
28.
Rosell R, Moran T, Queralt C, Porta R, Cardenal F, Camps C, Majem M, Lopez-Vivanco G, Isla D, Provencio M, et al. 2009. Screening for Epidermal Growth Factor Receptor Mutations in Lung Cancer. N Engl J Med. 361(10):958-967. https://doi.org/10.1056/nejmoa0904554
29.
Liu Z, Hou P, Ji M, Guan H, Studeman K, Jensen K, Vasko V, El-Naggar AK, Xing M. 2008. Highly Prevalent Genetic Alterations in Receptor Tyrosine Kinases and Phosphatidylinositol 3-Kinase/Akt and Mitogen-Activated Protein Kinase Pathways in Anaplastic and Follicular Thyroid Cancers. The Journal of Clinical Endocrinology & Metabolism. 93(8):3106-3116. https://doi.org/10.1210/jc.2008-0273
30.
Gao SP, Mark KG, Leslie K, Pao W, Motoi N, Gerald WL, Travis WD, Bornmann W, Veach D, Clarkson B, et al. 2007. Mutations in the EGFR kinase domain mediate STAT3 activation via IL-6 production in human lung adenocarcinomas. J. Clin. Invest.. 117(12):3846-3856. https://doi.org/10.1172/jci31871
31.
Fukushige S, Murotsu T, Matsubara K. 1986. Chromosomal assignment of human genes for gastrin, thyrotropin (TSH)-? subunit and C-erbB-2 by chromosome sorting combined with velocity sedimentation and southern hybridization. Biochemical and Biophysical Research Communications. 134(2):477-483. https://doi.org/10.1016/s0006-291x(86)80445-4
32.
Slamon D, Godolphin W, Jones L, Holt J, Wong S, Keith D, Levin W, Stuart S, Udove J, Ullrich A, et al. 1989. Studies of the HER-2/neu proto-oncogene in human breast and ovarian cancer. Science. 244(4905):707-712. https://doi.org/10.1126/science.2470152
33.
Qiu Y, Ravi L, Kung H. 1998. Requirement of ErbB2 for signalling by interleukin-6 in prostate carcinoma cells. Nature. 393(6680):83-85. https://doi.org/10.1038/30012
34.
Harskamp LR, Gansevoort RT, van Goor H, Meijer E. 2016. The epidermal growth factor receptor pathway in chronic kidney diseases. Nat Rev Nephrol. 12(8):496-506. https://doi.org/10.1038/nrneph.2016.91
35.
Scafidi J, Hammond TR, Scafidi S, Ritter J, Jablonska B, Roncal M, Szigeti-Buck K, Coman D, Huang Y, McCarter RJ, et al. 2014. Intranasal epidermal growth factor treatment rescues neonatal brain injury. Nature. 506(7487):230-234. https://doi.org/10.1038/nature12880
36.
Campbell P, Morton PE, Takeichi T, Salam A, Roberts N, Proudfoot LE, Mellerio JE, Aminu K, Wellington C, Patil SN, et al. 2014. Epithelial Inflammation Resulting from an Inherited Loss-of-Function Mutation in EGFR. Journal of Investigative Dermatology. 134(10):2570-2578. https://doi.org/10.1038/jid.2014.164
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