TY - JOUR
T1 - Growth Hormone-Releasing Hormone in Lung Physiology and Pulmonary Disease
AU - Zhang, Chongxu
AU - Cui, Tengjiao
AU - Cai, Renzhi
AU - Wangpaichitr, Medhi
AU - Mirsaeidi, Mehdi
AU - Schally, Andrew V.
AU - Jackson, Robert M.
N1 - Funding Information:
The TALENs were designed and constructed by Drs. Takashi Yamamoto and Tetsushi Sakuma (Hiroshima University, Hiroshima, Japan). Dr. Ken-Ichi Suzuki (Hirosima University) provided useful suggestions during the preparation of this chapter. This work was supported by JSPS KAKENHI and MEXT. We would like to thank Kyorin Corporation (Hyogo, Japan) for providing the feed for the newts.
PY - 2020/10/21
Y1 - 2020/10/21
N2 - Growth hormone-releasing hormone (GHRH) is secreted primarily from the hypothalamus, but other tissues, including the lungs, produce it locally. GHRH stimulates the release and secretion of growth hormone (GH) by the pituitary and regulates the production of GH and hepatic insulin-like growth factor-1 (IGF-1). Pituitary-type GHRH-receptors (GHRH-R) are expressed in human lungs, indicating that GHRH or GH could participate in lung development, growth, and repair. GHRH-R antagonists (i.e., synthetic peptides), which we have tested in various models, exert growth-inhibitory effects in lung cancer cells in vitro and in vivo in addition to having anti-inflammatory, anti-oxidative, and pro-apoptotic effects. One antagonist of the GHRH-R used in recent studies reviewed here, MIA-602, lessens both inflammation and fibrosis in a mouse model of bleomycin lung injury. GHRH and its peptide agonists regulate the proliferation of fibroblasts through the modulation of extracellular signal-regulated kinase (ERK) and Akt pathways. In addition to downregulating GH and IGF-1, GHRH-R antagonist MIA-602 inhibits signaling pathways relevant to inflammation, including p21-activated kinase 1-signal transducer and activator of transcription 3/nuclear factor-kappa B (PAK1-STAT3/NF-κB and ERK). MIA-602 induces fibroblast apoptosis in a dose-dependent manner, which is an effect that is likely important in antifibrotic actions. Taken together, the novel data reviewed here show that GHRH is an important peptide that participates in lung homeostasis, inflammation, wound healing, and cancer; and GHRH-R antagonists may have therapeutic potential in lung diseases.
AB - Growth hormone-releasing hormone (GHRH) is secreted primarily from the hypothalamus, but other tissues, including the lungs, produce it locally. GHRH stimulates the release and secretion of growth hormone (GH) by the pituitary and regulates the production of GH and hepatic insulin-like growth factor-1 (IGF-1). Pituitary-type GHRH-receptors (GHRH-R) are expressed in human lungs, indicating that GHRH or GH could participate in lung development, growth, and repair. GHRH-R antagonists (i.e., synthetic peptides), which we have tested in various models, exert growth-inhibitory effects in lung cancer cells in vitro and in vivo in addition to having anti-inflammatory, anti-oxidative, and pro-apoptotic effects. One antagonist of the GHRH-R used in recent studies reviewed here, MIA-602, lessens both inflammation and fibrosis in a mouse model of bleomycin lung injury. GHRH and its peptide agonists regulate the proliferation of fibroblasts through the modulation of extracellular signal-regulated kinase (ERK) and Akt pathways. In addition to downregulating GH and IGF-1, GHRH-R antagonist MIA-602 inhibits signaling pathways relevant to inflammation, including p21-activated kinase 1-signal transducer and activator of transcription 3/nuclear factor-kappa B (PAK1-STAT3/NF-κB and ERK). MIA-602 induces fibroblast apoptosis in a dose-dependent manner, which is an effect that is likely important in antifibrotic actions. Taken together, the novel data reviewed here show that GHRH is an important peptide that participates in lung homeostasis, inflammation, wound healing, and cancer; and GHRH-R antagonists may have therapeutic potential in lung diseases.
KW - antagonists
KW - bleomycin
KW - growth hormone-releasing hormone
KW - idiopathic pulmonary fibrosis
UR - http://www.scopus.com/inward/record.url?scp=85094684103&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85094684103&partnerID=8YFLogxK
U2 - 10.3390/cells9102331
DO - 10.3390/cells9102331
M3 - Review article
C2 - 33096674
AN - SCOPUS:85094684103
VL - 9
JO - Cells
JF - Cells
SN - 2073-4409
IS - 10
ER -