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Kallikrein-related peptidases in lung diseases
被引:19
|作者:
Bonda, Woodys Lenga Ma
[1
,2
]
Iochmann, Sophie
[1
,2
,3
]
Magnen, Melia
[1
,2
]
Courty, Yves
[1
,2
]
Reverdiau, Pascale
[1
,2
,3
]
机构:
[1] Ctr Etud Pathol Resp, INSERM, UMR 1100, Fac Med, 10 Blvd Tonnelle, F-37032 Tours, France
[2] Univ Tours, F-37032 Tours, France
[3] Univ Tours, IUT Tours, F-37082 Tours, France
关键词:
asthma;
cancer;
ECM remodelling;
influenza;
protease;
respiratory tract;
HUMAN TISSUE KALLIKREIN;
HUMAN AIRWAY EPITHELIUM;
GROWTH-FACTOR RECEPTOR;
PROTEINASE-ACTIVATED RECEPTORS;
OBSTRUCTIVE PULMONARY-DISEASE;
INFLUENZA-VIRUS SUBTYPES;
MESSENGER-RNA EXPRESSION;
SQUAMOUS-CELL CARCINOMA;
PROSTATE-CANCER;
IMMUNOHISTOCHEMICAL LOCALIZATION;
D O I:
10.1515/hsz-2018-0114
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Human tissue kallikreins (KLKs) are 15 members of the serine protease family and are present in various healthy human tissues including airway tissues. Multiple studies have revealed their crucial role in the pathophysiology of a number of chronic, infectious and tumour lung diseases. KLK1, 3 and 14 are involved in asthma pathogenesis, and KLK1 could be also associated with the exacerbation of this inflammatory disease caused by rhinovirus. KLK5 was demonstrated as an influenza virus activating protease in humans, and KLK1 and 12 could also be involved in the activation and spread of these viruses. KLKs are associated with lung cancer, with up-or downregulation of expression depending on the KLK, cancer subtype, stage of tumour and also the micro-environment. Functional studies showed that KLK12 is a potent pro-angiogenic factor. Moreover, KLK6 promotes malignant-cell proliferation and KLK13 invasiveness. In contrast, KLK8 and KLK10 reduce proliferation and invasion of malignant cells. Considering the involvement of KLKs in various physiological and pathological processes, KLKs appear to be potential biomarkers and therapeutic targets for lung diseases.
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页码:959 / 971
页数:13
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