2020
DOI: 10.1124/pr.120.019331
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International Union of Basic and Clinical Pharmacology. CIX. Differences and Similarities between Human and Rodent Prostaglandin E2Receptors (EP1–4) and Prostacyclin Receptor (IP): Specific Roles in Pathophysiologic Conditions

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Cited by 34 publications
(27 citation statements)
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References 845 publications
(1,228 reference statements)
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“…On the other hand, myeloid cell-­derived IGF1 also influences the outcomes of muscle regeneration through an autocrine effect, which regulates the transition of infiltrating macrophages from a M1 to a M2 phenotype [ 67 , 68 ]. Prostaglandin E2 (PGE2), another important immunosuppressive factor, can inhibit the proliferation of T cells, reduce the toxic effects of NK cells, and shape the functions and phenotypes of macrophages [ 69 71 ]. In addition, PGE2 also acts as a strong mitogen for MuSCs, through binding to the EP4 receptor on their own surface, triggering the intracellular cAMP/phosphor-CREB pathway and activating the proliferation-inducing transcription factor Nurr1 , ultimately robustly augmenting MuSC expansion [ 72 ].…”
Section: Regulation Of Myogenesis By Anti-inflammatory Responsesmentioning
confidence: 99%
“…On the other hand, myeloid cell-­derived IGF1 also influences the outcomes of muscle regeneration through an autocrine effect, which regulates the transition of infiltrating macrophages from a M1 to a M2 phenotype [ 67 , 68 ]. Prostaglandin E2 (PGE2), another important immunosuppressive factor, can inhibit the proliferation of T cells, reduce the toxic effects of NK cells, and shape the functions and phenotypes of macrophages [ 69 71 ]. In addition, PGE2 also acts as a strong mitogen for MuSCs, through binding to the EP4 receptor on their own surface, triggering the intracellular cAMP/phosphor-CREB pathway and activating the proliferation-inducing transcription factor Nurr1 , ultimately robustly augmenting MuSC expansion [ 72 ].…”
Section: Regulation Of Myogenesis By Anti-inflammatory Responsesmentioning
confidence: 99%
“…Several studies suggested that the mediators released from these adipose tissues can be involved in the pathogenesis of OA 33,34 . Prostanoids are released from adipose tissue and they are involved in pain and inflammation 13,22 . Therefore, we focused on the association between prostanoid levels and local fat pad thickness as well as other clinical parameters in knee OA patients.…”
Section: Discussionmentioning
confidence: 99%
“…Several studies including ours indicated that prostanoids were released from adipose tissue [13][14][15][16][17][18] and there are involved in the pathogenesis of obesity [19][20][21] . Among prostanoids, prostacyclin (PGI2) and thromboxane (TxA2) have opposite actions 22 . Therefore, TxA2/PGI2 ratio reflects the pathological condition 23 .…”
Section: Introductionmentioning
confidence: 99%
“…However, it should be noted that the addition of COX-2 inhibitor did not signi cantly affect the outcomes of randomized clinical trials of non-small cell lung cancer and colon cancer patients 30,31 . In PC, several in vivo and in vitro studies showed that anti-cancer effects including improvement of prognosis of COX-2 inhibitors were limited [32][33][34][35] . Thus, the chemopreventive and anti-cancer effects of COX-2 inhibitors in PC are still controversial.…”
Section: Discussionmentioning
confidence: 99%