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透明质酸酶:修订间差异

维基百科,自由的百科全书
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'''透明质酸酶'''(英语:Hyaluronidase,缩写:HAase)也称'''玻璃酸酶''',是[[催化]][[玻尿酸]](Hyaluronic acid,HA)降解的[[酶]]家族。Karl Meyer于1971年将这些酶根据酶反应产物分为三个不同的组。<ref>{{cite book|vauthors=Meyer K|chapter=Hyaluronidases|publisher=Academic Press|editor=Boyer PD|title=Enzymes|volume=V|date=1971|location=New York|pages=307–320|isbn=978-0-12-122705-0}}</ref>透明质酸酶的三种主要类型是两类真核内切糖苷酶[[水解酶]]和一类原核裂解酶型[[糖苷水解酶|糖苷酶]]。<ref>{{cite journal |vauthors=Stern R, Kogan G, Jedrzejas MJ, Soltés L |date=November 2007 |title=The many ways to cleave hyaluronan |journal=Biotechnology Advances |volume=25 |issue=6 |pages=537–57 |doi=10.1016/j.biotechadv.2007.07.001 |pmid=17716848}}</ref>
'''透明质酸酶'''(英语:Hyaluronidase,缩写:HAase)也称'''玻璃酸酶''',是[[催化]][[玻尿酸]](Hyaluronic acid,HA)降解的[[酶]]家族。Karl Meyer于1971年将这些酶根据酶反应产物分为三个不同的组。<ref>{{cite book|vauthors=Meyer K|chapter=Hyaluronidases|publisher=Academic Press|editor=Boyer PD|title=Enzymes|volume=V|date=1971|location=New York|pages=307–320|isbn=978-0-12-122705-0}}</ref>透明质酸酶的三种主要类型是两类真核内切糖苷酶[[水解酶]]和一类原核裂解酶型[[糖苷水解酶|糖苷酶]]。<ref>{{cite journal |vauthors=Stern R, Kogan G, Jedrzejas MJ, Soltés L |date=November 2007 |title=The many ways to cleave hyaluronan |journal=Biotechnology Advances |volume=25 |issue=6 |pages=537–57 |doi=10.1016/j.biotechadv.2007.07.001 |pmid=17716848}}</ref>


在[[人|人类]]中有六种透明质酸酶,其中五种是功能性透明质酸酶,即[[HYAL1]]、[[HYAL2]]、[[HYAL3]]、HYAL4和HYAL5(也称为[[SPAM1]]或PH-20),而第六种是一个[[假基因]],HYAL6(也称为HYALP1)。<ref name="ABC">{{cite journal |vauthors=Csóka AB, Scherer SW, Stern R |date=September 1999 |title=Expression analysis of six paralogous human hyaluronidase genes clustered on chromosomes 3p21 and 7q31 |journal=Genomics |volume=60 |issue=3 |pages=356–61 |doi=10.1006/geno.1999.5876 |pmid=10493834}}</ref><ref name="pmid11731267">{{cite journal |vauthors=Csoka AB, Frost GI, Stern R |date=December 2001 |title=The six hyaluronidase-like genes in the human and mouse genomes |journal=Matrix Biology |volume=20 |issue=8 |pages=499–508 |doi=10.1016/S0945-053X(01)00172-X |pmid=11731267}}</ref>HYAL1-3的[[基因]]集中在[[3號染色體|3号染色体]]上,而HYAL4-6的基因则集中在[[7號染色體|7号染色体]]上。<ref name="ABC" />HYAL1和HYAL2是大多数[[组织]]中主要的透明质酸酶。[[糖磷脂酰肌醇|GPI]]锚定的HYAL2负责裂解主要与[[CD44]]受体结合的高分子量玻尿酸。所产生的大小不一的玻尿酸片段在被内化到[[胞內體|内]][[溶酶体]]后被HYAL1进一步[[水解]],这会产生玻尿酸[[寡醣|寡糖]]。<ref name="Chanmee">{{cite journal |vauthors=Chanmee T, Ontong P, Itano N |date=May 2016 |title=Hyaluronan: A modulator of the tumor microenvironment |journal=Cancer Letters |volume=375 |issue=1 |pages=20–30 |doi=10.1016/j.canlet.2016.02.031 |pmid=26921785}}</ref>
在[[人|人类]]中有六种透明质酸酶,其中五种是功能性透明质酸酶,即[[HYAL1]]、[[HYAL2]]、[[HYAL3]]、HYAL4和HYAL5(也称为[[SPAM1]]或PH-20);第六种是一个[[假基因]],HYAL6(也称为HYALP1)。<ref name="ABC">{{cite journal |vauthors=Csóka AB, Scherer SW, Stern R |date=September 1999 |title=Expression analysis of six paralogous human hyaluronidase genes clustered on chromosomes 3p21 and 7q31 |journal=Genomics |volume=60 |issue=3 |pages=356–61 |doi=10.1006/geno.1999.5876 |pmid=10493834}}</ref><ref name="pmid11731267">{{cite journal |vauthors=Csoka AB, Frost GI, Stern R |date=December 2001 |title=The six hyaluronidase-like genes in the human and mouse genomes |journal=Matrix Biology |volume=20 |issue=8 |pages=499–508 |doi=10.1016/S0945-053X(01)00172-X |pmid=11731267}}</ref>HYAL1至HYAL3的[[基因]]集中在[[3號染色體|3号染色体]]上,而HYAL4至HYAL6的基因则集中在[[7號染色體|7号染色体]]上。<ref name="ABC" />HYAL1和HYAL2是大多数[[组织]]中主要的透明质酸酶。[[糖磷脂酰肌醇|GPI]]锚定的HYAL2负责裂解主要与[[CD44]]受体结合的高分子量HA。所产生的大小不一的HA片段在被内化到[[胞內體|内]][[溶酶体]]后被HYAL1进一步[[水解]],这会产生HA[[寡醣|寡糖]]。<ref name="Chanmee">{{cite journal |vauthors=Chanmee T, Ontong P, Itano N |date=May 2016 |title=Hyaluronan: A modulator of the tumor microenvironment |journal=Cancer Letters |volume=375 |issue=1 |pages=20–30 |doi=10.1016/j.canlet.2016.02.031 |pmid=26921785}}</ref>


透明质酸酶是一种酶促药物,根据其酶促机制它被分类为'''透明质酸葡萄糖苷酶家族'''(Hyaluronoglucosidases,{{EC number|3.2.1.35}}),可裂解[[N-乙酰葡糖胺]]和[[葡萄糖醛酸]]之间的 (1->4)-键。另外,透明质酸酶这个[[术语]]也可以指'''[[透明质酸葡糖醛酸酶]]'''(Hyaluronoglucuronidases,{{EC number|3.2.1.36}}),可裂解 (1->3)-键。除此之外,'''细菌透明质酸裂解酶'''(Bacterial hyaluronate lyases,{{EC number|4.2.2.1}})也可称为透明质酸酶,尽管这种情况并不常见。<ref>{{cite web|title=Hyaluronidase|url=http://enzyme.expasy.org/cgi-bin/enzyme/enzyme-search-de|access-date=17 November 2016|website=ENZYME|publisher=ExPASy}}</ref>
透明质酸酶是一种酶促药物,根据其酶促机制它被分类为'''透明质酸葡萄糖苷酶家族'''(Hyaluronoglucosidases,{{EC number|3.2.1.35}}),可裂解[[N-乙酰葡糖胺]]和[[葡萄糖醛酸]]之间的 (1->4)-键。另外,透明质酸酶这个[[术语]]也可以指'''[[透明质酸葡糖醛酸酶]]'''(Hyaluronoglucuronidases,{{EC number|3.2.1.36}}),可裂解 (1->3)-键。除此之外,'''细菌透明质酸裂解酶'''(Bacterial hyaluronate lyases,{{EC number|4.2.2.1}})也可称为透明质酸酶,尽管这种情况并不常见。<ref>{{cite web|title=Hyaluronidase|url=http://enzyme.expasy.org/cgi-bin/enzyme/enzyme-search-de|access-date=17 November 2016|website=ENZYME|publisher=ExPASy}}</ref>
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=== 医疗用途 ===
=== 医疗用途 ===
透明质酸酶催化玻尿酸([[细胞外基质]]的一种成分)的水解,导致玻尿酸的[[黏度|粘度]]降低,从而增加组织通透性。因此,它在医学上通常与其他[[药物]]一起使用,这样可以加速分散和输送。常见的应用是[[眼科学|眼科]][[外科学|手术]],与[[局部麻醉药|局部麻醉剂]]一起使用。它还能提高通过[[皮下注射]]给药的肠外液的吸收率,并且是皮下[[肾盂造影]]的辅助工具,以改善不透射线制剂的吸收。透明质酸酶还可用于高渗溶液的外渗。{{medcn|date=May 2020}}此外,透明質酸酶是一種被推薦的[[解毒剂|解毒劑]],用於[[长春花生物碱]]過量或外滲。<ref>{{cite web|date=September 2009|title=Chemotherapy extravasation guideline|url=http://www.beatson.scot.nhs.uk/content/mediaassets/doc/Extravasation%20guidance.pdf|access-date=4 June 2017|website=WOSCAN Cancer Nursing and Pharmacy Group}}</ref>
透明质酸酶催化HA([[细胞外基质]]的一种成分)的水解,导致HA的[[黏度|粘度]]降低,从而增加组织通透性。因此,它在医学上通常与其他[[药物]]一起使用,这样可以加速药物的分散和输送。透明质酸酶常见的应用是[[眼科学|眼科]][[外科学|手术]],与[[局部麻醉药|局部麻醉剂]]一起使用。它还能提高通过[[皮下注射]]给药的肠外液的吸收率,并且是皮下[[肾盂造影]]的辅助工具,以改善不透射线制剂的吸收。透明质酸酶还可用于高渗溶液的外渗。{{medcn|date=May 2020}}此外,透明質酸酶是一種被推薦的[[解毒剂|解毒劑]],用於[[长春花生物碱]]過量或外滲。<ref>{{cite web|date=September 2009|title=Chemotherapy extravasation guideline|url=http://www.beatson.scot.nhs.uk/content/mediaassets/doc/Extravasation%20guidance.pdf|access-date=4 June 2017|website=WOSCAN Cancer Nursing and Pharmacy Group}}</ref>


注射透明质酸酶可以溶解透明质酸类皮肤填充物,是寻求溶解唇部填充物或处理相关[[併發症|并发症]]的患者的最佳治疗选择。<ref>{{cite journal |vauthors=Borzabadi-Farahani A, Mosahebi A, Zargaran D |date=2022 |title=A Scoping Review of Hyaluronidase Use in Managing the Complications of Aesthetic Interventions |journal=Aesthetic Plastic Surgery. |doi=10.1007/s00266-022-03207-9 |pmid=36536092}}</ref> Patrick Treacy被认为是世界上第一批在这些类型的皮肤填充物引起的[[血管阻塞|血管闭塞]]期间使用透明质酸酶的医生之一,并为其使用建立了协议。<ref name="aestmedjourn">{{cite web|author=Anna Dobbie|title=Professor Patrick Treacy shortlisted for 2022 Irish Healthcare Award|url=https://aestheticmed.co.uk/site/shownewsdetails/professor-patrick-treacy-shortlisted-for-award|url-status=live|archive-date=30 October 2022|access-date=30 October 2022|publisher=Aesthetics Journal}}</ref>
注射透明质酸酶可以溶解透明质酸类皮肤填充物,是寻求溶解唇部填充物或处理相关[[併發症|并发症]]的患者的最佳治疗选择。<ref>{{cite journal |vauthors=Borzabadi-Farahani A, Mosahebi A, Zargaran D |date=2022 |title=A Scoping Review of Hyaluronidase Use in Managing the Complications of Aesthetic Interventions |journal=Aesthetic Plastic Surgery. |doi=10.1007/s00266-022-03207-9 |pmid=36536092}}</ref> Patrick Treacy被认为是世界上第一批在这些类型的皮肤填充物引起的[[血管阻塞|血管闭塞]]期间使用透明质酸酶的医生之一,并为其使用建立了协议。<ref name="aestmedjourn">{{cite web|author=Anna Dobbie|title=Professor Patrick Treacy shortlisted for 2022 Irish Healthcare Award|url=https://aestheticmed.co.uk/site/shownewsdetails/professor-patrick-treacy-shortlisted-for-award|url-status=live|archive-date=30 October 2022|access-date=30 October 2022|publisher=Aesthetics Journal}}</ref>
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2021年7月,FDA批准了达雷妥尤单抗/透明质酸酶-fihj与泊马度胺/地塞米松联合用于治疗成人多发性骨髓瘤。这些患者之前至少接受过一线治疗,包括[[来那度胺]]和[[蛋白酶体抑制剂]]。<ref>{{cite web|date=12 July 2021|title=FDA approves daratumumab and hyaluronidase-fihj with pomalidomide and|url=https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-daratumumab-and-hyaluronidase-fihj-pomalidomide-and-dexamethasone-multiple-myeloma|access-date=12 July 2021|website=U.S. [[Food and Drug Administration]] (FDA)}} {{PD-notice}}</ref>
2021年7月,FDA批准了达雷妥尤单抗/透明质酸酶-fihj与泊马度胺/地塞米松联合用于治疗成人多发性骨髓瘤。这些患者之前至少接受过一线治疗,包括[[来那度胺]]和[[蛋白酶体抑制剂]]。<ref>{{cite web|date=12 July 2021|title=FDA approves daratumumab and hyaluronidase-fihj with pomalidomide and|url=https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-daratumumab-and-hyaluronidase-fihj-pomalidomide-and-dexamethasone-multiple-myeloma|access-date=12 July 2021|website=U.S. [[Food and Drug Administration]] (FDA)}} {{PD-notice}}</ref>

== 在癌症中的作用 ==
由于观察出的结果相互矛盾,透明质酸酶在癌症中的作用历来存在争议<ref>{{cite journal |vauthors=Whatcott CJ, Han H, Posner RG, Hostetter G, Von Hoff DD |date=September 2011 |title=Targeting the tumor microenvironment in cancer: why hyaluronidase deserves a second look |journal=Cancer Discovery |volume=1 |issue=4 |pages=291–6 |doi=10.1158/2159-8290.CD-11-0136 |pmc=3204883 |pmid=22053288}}</ref>,即透明质酸酶(HYAL1/2)的水平在一些癌症中([[大腸癌|结直肠癌]]<ref>{{cite journal |display-authors=6 |vauthors=Bouga H, Tsouros I, Bounias D, Kyriakopoulou D, Stavropoulos MS, Papageorgakopoulou N, Theocharis DA, Vynios DH |date=September 2010 |title=Involvement of hyaluronidases in colorectal cancer |journal=BMC Cancer |publisher=Springer Nature |volume=10 |issue=1 |pages=499 |doi=10.1186/1471-2407-10-499 |pmc=2949809 |pmid=20849597}}</ref>、[[膀胱癌]]、[[前列腺癌]]、[[乳癌|乳腺癌]]和[[腦瘤|脑癌]])增加,然而,HYAL1的低表达则与[[胰臟癌|胰腺癌]]患者的生存率下降相关联。<ref name="Prognostic impact of hyaluronan and its regulators in pancreatic ductal adenocarcinoma">{{cite journal |vauthors=Cheng XB, Sato N, Kohi S, Yamaguchi K |date=2013 |title=Prognostic impact of hyaluronan and its regulators in pancreatic ductal adenocarcinoma |journal=PLOS ONE |volume=8 |issue=11 |pages=e80765 |bibcode=2013PLoSO...880765C |doi=10.1371/journal.pone.0080765 |pmc=3823618 |pmid=24244714 |doi-access=free}}</ref>这种明显相互矛盾的原因是HA的积累(由于[[透明质酸合成酶]](HAS)水平的增加和HYAL水平的降低),以及高HYAL水平将HA降解为HA寡糖,都会导致肿瘤恶性程度的增加。<ref name="Chanmee" />


== 参见 ==
== 参见 ==

2022年12月31日 (六) 10:08的版本

透明质酸酶
识别码
EC編號 3.2.1.35
CAS号 37326-33-3
数据库
IntEnz IntEnz浏览
BRENDA英语BRENDA BRENDA入口
ExPASy英语ExPASy NiceZyme浏览
KEGG KEGG入口
MetaCyc英语MetaCyc 代谢路径
PRIAM英语PRIAM_enzyme-specific_profiles 概述
PDB RCSB PDB PDBj PDBe PDBsum
基因本体 AmiGO / EGO
透明质酸酶
鑑定
標誌Hyaluronidase_1
PfamPF07212旧版
InterPro英语InterProIPR009860
透明质酸酶
鑑定
標誌Hyaluronidase_2
PfamPF07555旧版
InterPro英语InterProIPR011496

透明质酸酶(英语:Hyaluronidase,缩写:HAase)也称玻璃酸酶,是催化玻尿酸(Hyaluronic acid,HA)降解的家族。Karl Meyer于1971年将这些酶根据酶反应产物分为三个不同的组。[1]透明质酸酶的三种主要类型是两类真核内切糖苷酶水解酶和一类原核裂解酶型糖苷酶[2]

人类中有六种透明质酸酶,其中五种是功能性透明质酸酶,即HYAL1HYAL2HYAL3、HYAL4和HYAL5(也称为SPAM1或PH-20);第六种是一个假基因,HYAL6(也称为HYALP1)。[3][4]HYAL1至HYAL3的基因都集中在3号染色体上,而HYAL4至HYAL6的基因则集中在7号染色体上。[3]HYAL1和HYAL2是大多数组织中主要的透明质酸酶。GPI锚定的HYAL2负责裂解主要与CD44受体结合的高分子量HA。所产生的大小不一的HA片段在被内化到溶酶体后被HYAL1进一步水解,这会产生HA寡糖[5]

透明质酸酶是一种酶促药物,根据其酶促机制它被分类为透明质酸葡萄糖苷酶家族(Hyaluronoglucosidases,EC 3.2.1.35),可裂解N-乙酰葡糖胺葡萄糖醛酸之间的 (1->4)-键。另外,透明质酸酶这个术语也可以指透明质酸葡糖醛酸酶(Hyaluronoglucuronidases,EC 3.2.1.36),可裂解 (1->3)-键。除此之外,细菌透明质酸裂解酶(Bacterial hyaluronate lyases,EC 4.2.2.1)也可称为透明质酸酶,尽管这种情况并不常见。[6]

作为药物使用

透明质酸酶
臨床資料
读音/h(ə)ljuˌrɑːnɪˈds/[7]
商品名英语Drug nomenclatureHylenex, HyQvia, Vitrase, others
其他名稱hyaluronidase-fihj,hyaluronidase-oysk,hyaluronidase-zzxf,
透明质酸酶I-S,透明糖酶,透明质酸酶IV-S,玻璃酸酶
AHFS/Drugs.com专业药物信息
核准狀況
懷孕分級
  • : Exempt [8]
给药途径皮下注射
ATC碼
法律規範狀態
法律規範
识别信息
  • hyaluronidase
CAS号9001-54-1  checkY
DrugBank
ChemSpider
  • none
UNII
KEGG
ChEMBL
化学信息
化学式C2455H3775N617O704S21
摩尔质量53,871.08 g·mol−1

医疗用途

透明质酸酶催化HA(细胞外基质的一种成分)的水解,导致HA的粘度降低,从而增加组织通透性。因此,它在医学上通常与其他药物一起使用,这样可以加速药物的分散和输送。透明质酸酶常见的应用是在眼科手术,与局部麻醉剂一起使用。它还能提高通过皮下注射给药的肠外液的吸收率,并且是皮下肾盂造影的辅助工具,以改善不透射线制剂的吸收。透明质酸酶还可用于高渗溶液的外渗。[需要可靠醫學來源]此外,透明質酸酶是一種被推薦的解毒劑,用於长春花生物碱過量或外滲。[12]

注射透明质酸酶可以溶解透明质酸类皮肤填充物,是寻求溶解唇部填充物或处理相关并发症的患者的最佳治疗选择。[13] Patrick Treacy被认为是世界上第一批在这些类型的皮肤填充物引起的血管闭塞期间使用透明质酸酶的医生之一,并为其使用建立了协议。[14]

纯化和重组透明质酸酶

有四种不同的纯化透明质酸酶已被批准在美国使用,其中三种是来源于动物的,而一种是重组的。在皮下肾盂造影术中,它们被用作皮下输液的辅助剂,以实现水合作用,增加其他注射药物的分散和吸收,或改善不透射线药物的再吸收。[15][16][17]

这三种天然来源的透明质酸酶是从睾丸制剂中获得的人类HYAL5的同源物。它们以商品名Vitrase(源自绵羊FDA于2004年5月批准)[18]Amphadase(源自,FDA于2004年10月批准)[19]Hydase(源自牛,FDA于2005年10月批准)出售。[20]

重组人透明质酸酶(Hylenex)于2005年12月获准在美国使用[21][22],它相当于人类HYAL5的可溶性片段,由含有编码该酶的DNA质粒的基因工程中国仓鼠卵巢细胞(CHO)培养物中产生。[23]

组合疗法

一种重组人透明质酸酶试剂盒,HyQvia,于2013年5月获准在欧盟使用[24],并于2014年9月在获准在美国使用。[25][26]它是一个双瓶单元,包含一瓶10%的抗体输液(人)和一瓶重组人透明质酸酶。[27]它是一种含有重组人透明质酸酶的抗体,在美国适用于治疗成人原发性免疫缺陷症。这包括但不限于常见的变异型免疫缺陷X-连锁无丙种球蛋白血症、先天性丙种球蛋白血症、维斯科特·奥尔德里奇综合征和严重联合免疫缺陷。[27]

在欧盟,它被指定为成人、儿童和青少年(0-18岁)的替代疗法:

使用Hylenex的皮下注射免疫球蛋白(SCIG)会使SCIG的注射量远远大于通常可能的皮下注射。这提供了一种可以按月来注射的SCIG形式,比其他形式的SCIG允许的时间更长。使用HyQvia的全身不良反应率高于传统的SCIG,但低于静脉注射免疫球蛋白(IVIG)患者的典型不良反应。[28]它也用于硬膜外粘连松解术以进行疼痛管理。[需要可靠醫學來源]

在美国,透明质酸酶可用于一些固定剂量组合药物产品,例如:利妥昔单抗/透明质酸酶(Rituxan Hycela)、曲妥珠单抗/透明质酸酶-oysk(Herceptin Hylecta)、达雷妥尤单抗/透明质酸酶-fihj(Darzalex Faspro)和帕妥珠单抗/曲妥珠单抗/透明质酸酶-zzxf(Phesgo)。[29][30][31][32][33][34][35]

2021年7月,FDA批准了达雷妥尤单抗/透明质酸酶-fihj与泊马度胺/地塞米松联合用于治疗成人多发性骨髓瘤。这些患者之前至少接受过一线治疗,包括来那度胺蛋白酶体抑制剂[36]

在癌症中的作用

由于观察出的结果相互矛盾,透明质酸酶在癌症中的作用历来存在争议[37],即透明质酸酶(HYAL1/2)的水平在一些癌症中(结直肠癌[38]膀胱癌前列腺癌乳腺癌脑癌)增加,然而,HYAL1的低表达则与胰腺癌患者的生存率下降相关联。[39]这种明显相互矛盾的原因是HA的积累(由于透明质酸合成酶(HAS)水平的增加和HYAL水平的降低),以及高HYAL水平将HA降解为HA寡糖,都会导致肿瘤恶性程度的增加。[5]

参见

参考文献

  1. ^ Meyer K. Hyaluronidases. Boyer PD (编). Enzymes V. New York: Academic Press. 1971: 307–320. ISBN 978-0-12-122705-0. 
  2. ^ Stern R, Kogan G, Jedrzejas MJ, Soltés L. The many ways to cleave hyaluronan. Biotechnology Advances. November 2007, 25 (6): 537–57. PMID 17716848. doi:10.1016/j.biotechadv.2007.07.001. 
  3. ^ 3.0 3.1 Csóka AB, Scherer SW, Stern R. Expression analysis of six paralogous human hyaluronidase genes clustered on chromosomes 3p21 and 7q31. Genomics. September 1999, 60 (3): 356–61. PMID 10493834. doi:10.1006/geno.1999.5876. 
  4. ^ Csoka AB, Frost GI, Stern R. The six hyaluronidase-like genes in the human and mouse genomes. Matrix Biology. December 2001, 20 (8): 499–508. PMID 11731267. doi:10.1016/S0945-053X(01)00172-X. 
  5. ^ 5.0 5.1 Chanmee T, Ontong P, Itano N. Hyaluronan: A modulator of the tumor microenvironment. Cancer Letters. May 2016, 375 (1): 20–30. PMID 26921785. doi:10.1016/j.canlet.2016.02.031. 
  6. ^ Hyaluronidase. ENZYME. ExPASy. [17 November 2016]. 
  7. ^ hyaluronidase. Merriam-Webster Dictionary. [2020-07-03]. 
  8. ^ 8.0 8.1 Hyaluronidase Use During Pregnancy. Drugs.com. 14 June 2019 [3 February 2020]. 
  9. ^ ARTG ID 27749 Hyalase 1500IU powder for injection ampoule. Therapeutic Goods Administration (TGA). [9 August 2020]. 
  10. ^ Hyalase 1500 I.U. Powder for Solution for Injection/Infusion or Hyaluronidase 1500 I.U. Powder for Solution for Injection/Infusion - Summary of Product Characteristics (SmPC). (emc). 12 March 2015 [1 May 2020]. 
  11. ^ HyQvia 100 mg/ml solution for infusion for subcutaneous use - Summary of Product Characteristics (SmPC). (emc). 15 January 2020 [1 May 2020]. 
  12. ^ Chemotherapy extravasation guideline (PDF). WOSCAN Cancer Nursing and Pharmacy Group. September 2009 [4 June 2017]. 
  13. ^ Borzabadi-Farahani A, Mosahebi A, Zargaran D. A Scoping Review of Hyaluronidase Use in Managing the Complications of Aesthetic Interventions. Aesthetic Plastic Surgery. 2022. PMID 36536092. doi:10.1007/s00266-022-03207-9. 
  14. ^ Anna Dobbie. Professor Patrick Treacy shortlisted for 2022 Irish Healthcare Award. Aesthetics Journal. [30 October 2022]. 
  15. ^ Vitrase-hyaluronidase, ovine injection, solution. DailyMed. 29 May 2018 [1 May 2020]. 
  16. ^ Amphadase- hyaluronidase injection. DailyMed. 28 November 2016 [1 May 2020]. 
  17. ^ Hydase- hyaluronidase injection, solution. DailyMed. 16 November 2015 [1 May 2020]. 
  18. ^ Drug Approval Package: Vitrase (Hyaluronidase) NDA #021640. U.S. Food and Drug Administration (FDA). 15 November 2004 [1 May 2020]. 
  19. ^ Drug Approval Package: Amphadase (Hyaluronidase) NDA #021665. U.S. Food and Drug Administration (FDA). 4 February 2005 [1 May 2020]. 
  20. ^ Hydase: FDA-Approved Drugs. U.S. Food and Drug Administration (FDA). 23 March 2020 [1 May 2020]. 
  21. ^ Drug Approval Package: Hylenex Recombinant (Hyaluronidase) NDA #021859. U.S. Food and Drug Administration (FDA). 3 January 2006 [1 May 2020]. 
  22. ^ Halozyme Therapeutics and Baxter Healthcare Corporation Announce FDA Approval of Hylenex. [2008-11-07]. (原始内容存档于October 18, 2007). 
  23. ^ Hylenex recombinant (hyaluronidase- human recombinant injection), solution. DailyMed. 1 January 2016 [1 May 2020]. 
  24. ^ 24.0 24.1 24.2 24.3 24.4 HyQvia EPAR. European Medicines Agency (EMA). [1 May 2020].  Text was copied from this source which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  25. ^ Hyqvia. U.S. Food and Drug Administration (FDA). 27 February 2015 [1 May 2020]. (原始内容存档于22 July 2017). 
  26. ^ Hyqvia Approval Letter. U.S. Food and Drug Administration (FDA). [20 November 2015]. (原始内容存档于22 July 2017). 
  27. ^ 27.0 27.1 Hyqvia (immune globulin 10 percent- human with recombinant human hyaluronidase) kit. DailyMed. [1 May 2020]. 
  28. ^ Sanford M. Human immunoglobulin 10 % with recombinant human hyaluronidase: replacement therapy in patients with primary immunodeficiency disorders. BioDrugs. August 2014, 28 (4): 411–20. PMID 24925799. S2CID 8091134. doi:10.1007/s40259-014-0104-3. 
  29. ^ Drug Approval Package: Rituxan Hycela. U.S. Food and Drug Administration (FDA). 11 October 2018 [1 May 2020]. 
  30. ^ Rituxan Hycela- rituximab and hyaluronidase injection, solution. DailyMed. 3 December 2019 [1 May 2020]. 
  31. ^ Drug Approval Package: Herceptin Hylecta. U.S. Food and Drug Administration (FDA). 17 October 2019 [1 May 2020]. 
  32. ^ Herceptin Hylecta- trastuzumab and hyaluronidase-oysk injection, solution. DailyMed. 13 May 2019 [1 May 2020]. 
  33. ^ Darzalex Faspro: FDA-Approved Drugs. U.S. Food and Drug Administration (FDA). [1 May 2020]. 
  34. ^ FDA Approves Breast Cancer Treatment That Can Be Administered At Home By Health Care Professional. U.S. Food and Drug Administration (新闻稿). 29 June 2020 [29 June 2020]. 
  35. ^ FDA approves combination of pertuzumab, trastuzumab, and hyaluronidase. U.S. Food and Drug Administration (FDA). 29 June 2020 [29 June 2020]. 
  36. ^ FDA approves daratumumab and hyaluronidase-fihj with pomalidomide and. U.S. Food and Drug Administration (FDA). 12 July 2021 [12 July 2021].  公有领域 本文含有此來源中屬於公有领域的内容。
  37. ^ Whatcott CJ, Han H, Posner RG, Hostetter G, Von Hoff DD. Targeting the tumor microenvironment in cancer: why hyaluronidase deserves a second look. Cancer Discovery. September 2011, 1 (4): 291–6. PMC 3204883可免费查阅. PMID 22053288. doi:10.1158/2159-8290.CD-11-0136. 
  38. ^ Bouga H, Tsouros I, Bounias D, Kyriakopoulou D, Stavropoulos MS, Papageorgakopoulou N, et al. Involvement of hyaluronidases in colorectal cancer. BMC Cancer (Springer Nature). September 2010, 10 (1): 499. PMC 2949809可免费查阅. PMID 20849597. doi:10.1186/1471-2407-10-499. 
  39. ^ Cheng XB, Sato N, Kohi S, Yamaguchi K. Prognostic impact of hyaluronan and its regulators in pancreatic ductal adenocarcinoma. PLOS ONE. 2013, 8 (11): e80765. Bibcode:2013PLoSO...880765C. PMC 3823618可免费查阅. PMID 24244714. doi:10.1371/journal.pone.0080765可免费查阅. 

外部链接