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HER2/neu

HER2/neu
已知的結構
PDB直系同源搜索: PDBe RCSB
識別號
别名ERBB2;, CD340, HER-2, HER-2/neu, HER2, MLN 19, NEU, NGL, TKR1, erb-b2 receptor tyrosine kinase 2
外部IDOMIM164870 MGI95410 HomoloGene3273 GeneCardsERBB2
EC number2.7.10.1
相關疾病
breast carcinoma、​disease of cellular proliferation、​非小細胞肺癌[1]
為以下藥物的標靶
阿法替尼、​canertinib、​達科米替尼、​拉帕替尼、​mubritinib、​来那替尼、​玛格妥昔单抗、​達科米替尼、​帕妥珠单抗、​图卡替尼、​bms-599626、​bms-690514、​cp-724714、​cudc-101、​poziotinib、​sapitinib、​varlitinib、​tesevatinib[2]
基因位置(人类
17號染色體
染色体17號染色體[3]
17號染色體
HER2/neu的基因位置
HER2/neu的基因位置
基因座17q12起始39,687,914 bp[3]
终止39,730,426 bp[3]
RNA表达模式


查阅更多表达数据
直系同源
物種人類小鼠
Entrez
Ensembl
UniProt
mRNA​序列

​NM_001005862
​NM_001289936
​NM_001289937
​NM_001289938
​NM_004448

NM_001003817
​NM_010152

蛋白序列

NP_001003817

基因位置​(UCSC)Chr 17: 39.69 – 39.73 MbChr 11: 98.3 – 98.33 Mb
PubMed​查找[5][6]
維基數據
檢視/編輯人類檢視/編輯小鼠

人类表皮生长因子受体2(英語:human epidermal growth factor receptor 2缩写HER2,亦称为NeuErbB-2CD340分化群340)或p185)是一种由ERBB2基因编码的蛋白质。HER2是表皮生长因子受体(EGFR/ErbB)家族的成员。

功能

HER2是结合在细胞膜表面的受体酪氨酸激酶,参与导致细胞生长和分化的訊息傳遞途径,由原癌基因HER2/neu编码。一般认为HER2是一个孤受体,表皮生长因子家族的配体都不能激活它。但配体结合ErbB受体时可形成二聚体,且HER2可与ErbB家族的其他成员结合成异二聚体。[7]HER2基因是原癌基因,位于人类17号染色体长臂(17q21-q22)。[8]

與癌症的關係

HER-2基因是影響乳癌預後的一個重要因素,大約有25%-30%左右的乳癌患者,受到體內癌細胞HER-2基因過量表現的影響,他們的癌細胞不僅繁殖能力強,對部份化學治療藥物也容易有抗藥性,造成病患即使接受手術治療,癌細胞仍然有較高復發及轉移的機率,無法長期存活。

乳癌病患可分為Her-2/neu陽性或Her-2/neu陰性兩種截然不同的預後之乳癌。乳癌患者的腫瘤,若HER-2蛋白質出現過量表現,這類的腫瘤生長速度較快且生物行為較為惡性,使得手術後復發率高於其他類型的乳癌。[9]

表皮生長因子受體(EGFR)信號傳導級聯

針对HER2的葯物

羅氏藥廠開發的賀癌平(Herceptin)即是以HER2為标靶的葯物,對晚期转移性的乳腺癌頗具效用。

  1. 重组型人源化单克隆抗体 Trastuzumab (Herceptin®), 是IgG1 monoclonal antibody,可透過結合到乳癌細胞膜上的HER2 receptor的Domain4去抑制下游的hetero- and homodimerization和信號傳遞。;
  2. 完全人源化单克隆抗体 Pertuzumab (Perjeta®),和Trastuzumab藥理作用位點相似,但Pertuzumab 是結合在HER2的Domain2,去抑制下游路徑,而且因為Domain2是屬於extracellular receptor dimerization,因此可防止其他的HER family members和HER2進行dimerization,從而抑制了ligand-induced signaling,抑制了細胞生長而進行細胞凋亡,其中HER2/HER3被认为是下游通路激活的最强二聚体;
  3. 单抗结合型药物 Ado-Trastuzumab emtansine (Kadcyla®),為新藥,是一種Antibody和Drug的conjugate(ADC)。Trastuzumab上述已介紹過他的作用位點,而新藥T-DM1則是將Trastuzumab和maytansine 1用thioether鍵結起來,DM1即derivative of maytansine 1,是一種合成Microtubule 過程中dimerization的抑制劑,將Trastuzumab和cytotoxic agent DM1結合,除了有Trastuzumab本身能夠與HER2 receptor Domain4結合,進而停止了癌細胞的生長,DM1透過receptor-mediated進入細胞內作用,並在lysosome內代謝,釋放出含DM1的代謝產物,此物質可結合在Microtubule上,導致有絲分裂終止和細胞死亡。[10]
  4. Neratinib,為口服製劑,irreversible inhibitor,抑制HER2 and EGFR protein tyrosine kinase(TK)。[11]
  5. 酪氨酸激酶抑制剂 Lapatinib Ditosylate (Tykerb®),口服製劑,和Neratinib相似,一樣是EGFR and HER2 tyrosine kinase的抑制劑。[11]
  6. mTOR 抑制剂 Everolimus (Afinitor®)

相互作用

参考文献

  1. ^ 與HER2/neu相關的疾病;在維基數據上查看/編輯參考. 
  2. ^ 對人类表皮生长因子受体II起作用的藥物;在維基數據上查看/編輯參考. 
  3. ^ 3.0 3.1 3.2 GRCh38: Ensembl release 89: ENSG00000141736 - Ensembl, May 2017
  4. ^ 4.0 4.1 4.2 GRCm38: Ensembl release 89: ENSMUSG00000062312 - Ensembl, May 2017
  5. ^ Human PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine. 
  6. ^ Mouse PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine. 
  7. ^ Olayioye MA. Update on HER-2 as a target for cancer therapy: intracellular signaling pathways of ErbB2/HER-2 and family members. Breast Cancer Res. 2001, 3 (6): 385–389. PMID 11737890. doi:10.1186/bcr327. 
  8. ^ Coussens L. Tyrosine Kinase Receptor with Extensive Homology to EGF Receptor Shares Chromosomal Location with neu Oncogene. Science. 1985, 230: 1132–1139. doi:10.1126/science.2999974. 
  9. ^ HER-2陽性早期乳癌治療的近況. 台灣癌症防治網. 2009年10月16日 [2009-10-06]. (原始内容存档于2011年5月25日). 
  10. ^ Sadeghi, S., Olevsky, O., & Hurvitz, S. A. (2014). Profiling and targeting HER2-positive breast cancer using trastuzumab emtansine. Pharmacogenomics and personalized medicine, 7, 329.
  11. ^ 11.0 11.1 Goodman, L. S. (1996). Goodman and Gilman's the pharmacological basis of therapeutics (Vol. 1549). New York: McGraw-Hill.P.1208

深入阅读

  • Ross JS, Fletcher JA, Linette GP; et al. The Her-2/neu gene and protein in breast cancer 2003: biomarker and target of therapy. Oncologist. 2003, 8 (4): 307–25. PMID 12897328. doi:10.1634/theoncologist.8-4-307. 
  • Zhou BP, Hung MC. Dysregulation of cellular signaling by HER2/neu in breast cancer. Semin. Oncol. 2003, 30 (5 Suppl 16): 38–48. PMID 14613025. doi:10.1053/j.seminoncol.2003.08.006. 
  • Ménard S, Casalini P, Campiglio M; et al. Role of HER2/neu in tumor progression and therapy. Cell. Mol. Life Sci. 2005, 61 (23): 2965–78. PMID 15583858. doi:10.1007/s00018-004-4277-7. 
  • Becker JC, Muller-Tidow C, Serve H; et al. Role of receptor tyrosine kinases in gastric cancer: new targets for a selective therapy. World J. Gastroenterol. 2006, 12 (21): 3297–305. PMID 16733844. 
  • Laudadio J, Quigley DI, Tubbs R, Wolff DJ. HER2 testing: a review of detection methodologies and their clinical performance. Expert Rev. Mol. Diagn. 2007, 7 (1): 53–64. PMID 17187484. doi:10.1586/14737159.7.1.53. 
  • Bianchi F, Tagliabue E, Ménard S, Campiglio M. Fhit expression protects against HER2-driven breast tumor development: unraveling the molecular interconnections. Cell Cycle. 2007, 6 (6): 643–6. PMID 17374991. doi:10.4161/cc.6.6.4033. 
  • Del Bimbo A., Meoni M., Pala P. Accurate evaluation of HER-2 amplification in FISH images. Imaging Systems and Techniques (IST), 2010 IEEE International Conference on. 2010: 407–10. ISBN 978-1-4244-6492-0. doi:10.1109/IST.2010.5548461. 

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