[1] |
PIVONELLO R, DE LEO M, COZZOLINO A,et al. The treatment of Cushing's disease[J]. Endocr Rev, 2015, 36(4):385-486. DOI: 10.1210/er.2013-1048.
|
[2] |
LUQUE R M, GAHETE M D, HOCHGESCHWENDER U,et al. Evidence that endogenous SST inhibits ACTH and ghrelin expression by independent pathways[J]. Am J Physiol Endocrinol Metab, 2006, 291(2):E395-403. DOI: 10.1152/ajpendo.00038.2006.
|
[3] |
COLAO A, PETERSENN S, NEWELL-PRICE J,et al. A 12-month phase 3 study of pasireotide in Cushing's disease[J]. N Engl J Med, 2012, 366(10):914-924. DOI: 10.1056/nejmoa1105743.
|
[4] |
SCHOPOHL J, GU F, RUBENS R,et al. Pasireotide can induce sustained decreases in urinary cortisol and provide clinical benefit in patients with Cushing's disease:results from an open-ended,open-label extension trial[J]. Pituitary, 2015, 18(5):604-612. DOI: 10.1007/s11102-014-0618-1.
|
[5] |
LACROIX A, GU F, GALLARDO W,et al. Efficacy and safety of once-monthly pasireotide in Cushing's disease:a 12 month clinical trial[J]. Lancet Diabetes Endocrinol, 2018, 6(1):17-26. DOI: 10.1016/s2213-8587(17)30326-1.
|
[6] |
FLESERIU M, PETERSENN S, BILLER B M K,et al. Long-term efficacy and safety of once-monthly pasireotide in Cushing's disease:a Phase Ⅲ extension study[J]. Clin Endocrinol:Oxf, 2019, 91(6):776-785. DOI: 10.1111/cen.14081.
|
[7] |
PAWLIKOWSKI M, KUNERT-RADEK J, STEPIE H. Direct antiproliferative effect of dopamine agonists on the anterior pituitary gland in organ culture[J]. J Endocrinol, 1978, 79(2):245-246. DOI: 10.1677/joe.0.0790245.
|
[8] |
WANG Y W, LI J Y, TOHTI M,et al. The expression profile of Dopamine D2 receptor,MGMT and VEGF in different histological subtypes of pituitary adenomas:a study of 197 cases and indications for the medical therapy[J]. J Exp Clin Cancer Res, 2014, 33:56. DOI: 10.1186/s13046-014-0056-y.
|
[9] |
FERONE D, PIVONELLO C, VITALE G,et al. Molecular basis of pharmacological therapy in Cushing's disease[J]. Endocrine, 2014, 46(2):181-198. DOI: 10.1007/s12020-013-0098-5.
|
[10] |
FEELDERS R A, NEWELL-PRICE J, PIVONELLO R,et al. Advances in the medical treatment of Cushing's syndrome[J]. Lancet Diabetes Endocrinol, 2019, 7(4):300-312. DOI: 10.1016/s2213-8587(18)30155-4.
|
[11] |
PIVONELLO R, DE MARTINO M C, CAPPABIANCA P,et al. The medical treatment of Cushing's disease:effectiveness of chronic treatment with the dopamine agonist cabergoline in patients unsuccessfully treated by surgery[J]. J Clin Endocrinol Metab, 2009, 94(1):223-230. DOI: 10.1210/jc.2008-1533.
|
[12] |
FERRIERE A, CORTET C, CHANSON P,et al. Cabergoline for Cushing's disease:a large retrospective multicenter study[J]. Eur J Endocrinol, 2017, 176(3):305-314. DOI: 10.1530/eje-16-0662.
|
[13] |
NAKHLEH A, SAIEGH L, REUT M,et al. Cabergoline treatment for recurrent Cushing's disease during pregnancy[J]. Hormones:Athens, 2016, 15(3):453-458. DOI: 10.14310/horm.2002.1685.
|
[14] |
FERONE D, GATTO F, ARVIGO M,et al. The clinical-molecular interface of somatostatin,dopamine and their receptors in pituitary pathophysiology[J]. J Mol Endocrinol, 2009, 42(5):361-370. DOI: 10.1677/jme-08-0162.
|
[15] |
VáZQUEZ-BORREGO M C, L-LóPEZ F, GáLVEZ-MORENO M A,et al. A new generation somatostatin-dopamine analogue exerts potent antitumoral actions on pituitary neuroendocrine tumor cells[J]. Neuroendocrinology, 2020, 110(1/2):70-82. DOI: 10.1159/000500812.
|
[16] |
GüNTHER T, TULIPANO G, DOURNAUD P,et al. International union of basic and clinical pharmacology. CV. somatostatin receptors:structure,function,ligands,and new nomenclature[J]. Pharmacol Rev, 2018, 70(4):763-835. DOI: 10.1124/pr.117.015388.
|
[17] |
ALBANI A, PEREZ-RIVAS L G, REINCKE M,et al. Pathogenesis of cushing disease:an update on the genetics of corticotropinomas[J]. Endocr Pract, 2018, 24(10):907-914. DOI: 10.4158/ep-2018-0111.
|
[18] |
LIU N A, JIANG H, BEN-SHLOMO A,et al. Targeting zebrafish and murine pituitary corticotroph tumors with a cyclin-dependent kinase (CDK) inhibitor[J]. PNAS, 2011, 108(20):8414-8419. DOI: 10.1073/pnas.1018091108.
|
[19] |
ARAKI T, LIU N A. Cell cycle regulators and lineage-specific therapeutic targets for cushing disease[J]. Front Endocrinol:Lausanne, 2018, 9:444. DOI: 10.3389/fendo.2018.00444.
|
[20] |
LIU N A, ARAKI T, CUEVAS-RAMOS D,et al. Cyclin E-mediated human proopiomelanocortin regulation as a therapeutic target for cushing disease[J]. J Clin Endocrinol Metab, 2015, 100(7):2557-2564. DOI: 10.1210/jc.2015-1606.
|
[21] |
THEODOROPOULOU M, ARZBERGER T, GRUEBLER Y,et al. Expression of epidermal growth factor receptor in neoplastic pituitary cells:evidence for a role in corticotropinoma cells[J]. J Endocrinol, 2004, 183(2):385-394. DOI: 10.1677/joe.1.05616.
|
[22] |
CHANDRA P, RAJARAM P, TICKU S,et al. Epidermal growth factor receptor:Role in human cancer[J]. Indian J Dent Res, 2017, 28(6):687. DOI: 10.4103/ijdr.ijdr_534_16.
|
[23] |
TATSI C, FLIPPO C, STRATAKIS C A. Cushing syndrome:Old and new genes[J]. Best Pract Res Clin Endocrinol Metab, 2020, 34(2):101418. DOI: 10.1016/j.beem.2020.101418.
|
[24] |
PEREZ-RIVAS L G, THEODOROPOULOU M, FERRAù F,et al. The gene of the ubiquitin-specific protease 8 is frequently mutated in adenomas causing Cushing's disease[J]. J Clin Endocrinol Metab, 2015, 100(7):E997-1004. DOI: 10.1210/jc.2015-1453.
|
[25] |
FOULKES E, NEWELL-PRICE J. New molecular targets for treatment of Cushing's disease[J]. Endocrinol Metab Clin North Am, 2018, 47(2):367-373. DOI: 10.1016/j.ecl.2018.02.006.
|
[26] |
FUKUOKA H, COOPER O, BEN-SHLOMO A,et al. EGFR as a therapeutic target for human,canine,and mouse ACTH-secreting pituitary adenomas[J]. J Clin Invest, 2011, 121(12):4712-4721. DOI: 10.1172/jci60417.
|
[27] |
SESHACHARYULU P, PONNUSAMY M P, HARIDAS D,et al. Targeting the EGFR signaling pathway in cancer therapy[J]. Expert Opin Ther Targets, 2012, 16(1):15-31. DOI: 10.1517/14728222.2011.648617.
|
[28] |
ASARI Y, KAGEYAMA K, SUGIYAMA A,et al. Lapatinib decreases the ACTH production and proliferation of corticotroph tumor cells[J]. Endocr J, 2019, 66(6):515-522. DOI: 10.1507/endocrj.ej18-0491.
|
[29] |
CIATO D, ALBANI A. Molecular mechanisms of glucocorticoid resistance in corticotropinomas:new developments and drug targets[J]. Front Endocrinol:Lausanne, 2020, 11:21. DOI: 10.3389/fendo.2020.00021.
|
[30] |
RIEBOLD M, KOZANY C, FREIBURGER L,et al. A C-terminal HSP90 inhibitor restores glucocorticoid sensitivity and relieves a mouse allograft model of Cushing disease[J]. Nat Med, 2015, 21(3):276-280. DOI: 10.1038/nm.3776.
|
[31] |
SHEN Y, JI C, JIAN X,et al. Regulation of the EGFR pathway by HSP90 is involved in the pathogenesis of Cushing's disease[J]. Front Endocrinol:Lausanne, 2020, 11:601984. DOI: 10.3389/fendo.2020.601984.
|
[32] |
|
[33] |
SALMANINEJAD A, VALILOU S F, SHABGAH A G,et al. PD-1/PD-L1 pathway:Basic biology and role in cancer immunotherapy[J]. J Cell Physiol, 2019, 234(10):16824-16837. DOI: 10.1002/jcp.28358.
|
[34] |
HOFMEYER K A, JEON H, ZANG X X. The PD-1/PD-L1 (B7-H1) pathway in chronic infection-induced cytotoxic T lymphocyte exhaustion[J]. J Biomed Biotechnol, 2011, 2011:451694. DOI: 10.1155/2011/451694.
|
[35] |
|
[36] |
WANG P F, WANG T J, YANG Y K,et al. The expression profile of PD-L1 and CD 8+ lymphocyte in pituitary adenomas indicating for immunotherapy[J]. J Neurooncol, 2018, 139(1):89-95. DOI: 10.1007/s11060-018-2844-2.
|
[37] |
KEMENY H R, ELSAMADICY A A, FARBER S H,et al. Targeting PD-L1 initiates effective antitumor immunity in a murine model of cushing disease[J]. Clin Cancer Res, 2020, 26(5):1141-1151. DOI: 10.1158/1078-0432.CCR-18-3486.
|
[38] |
LIN A L, JONSSON P, TABAR V,et al. Marked response of a hypermutated ACTH-secreting pituitary carcinoma to ipilimumab and nivolumab[J]. J Clin Endocrinol Metab, 2018, 103(10):3925-3930. DOI: 10.1210/jc.2018-01347.
|
[39] |
CACCESE M, BARBOT M, CECCATO F,et al. Rapid disease progression in patient with mismatch-repair deficiency pituitary ACTH-secreting adenoma treated with checkpoint inhibitor pembrolizumab[J]. Anticancer Drugs, 2020, 31(2):199-204. DOI: 10.1097/cad.0000000000000856.
|
[40] |
SCHRECK K C,GROSSMAN S A. Role of temozolomide in the treatment of cancers involving the central nervous system[J]. Oncology:Williston Park,2018,32(11):555-560,569.
|
[41] |
SHEEHAN J, RAINEY J, NGUYEN J,et al. Temozolomide-induced inhibition of pituitary adenoma cells[J]. J Neurosurg, 2011, 114(2):354-358. DOI: 10.3171/2010.4.jns1024.
|
[42] |
RAVEROT G, CASTINETTI F, JOUANNEAU E,et al. Pituitary carcinomas and aggressive pituitary tumours:merits and pitfalls of temozolomide treatment[J]. Clin Endocrinol:Oxf, 2012, 76(6):769-775. DOI: 10.1111/j.1365-2265.2012.04381.x.
|
[43] |
BROSSAUD J, PALLET V, CORCUFF J B. Vitamin A,endocrine tissues and hormones:interplay and interactions[J]. Endocr Connect, 2017, 6(7):R121-130. DOI: 10.1530/ec-17-0101.
|
[44] |
CASTILLO V, GIACOMINI D, PA'EZ-PEREDA M,et al. Retinoic acid as a novel medical therapy for Cushing's disease in dogs[J]. Endocrinology, 2006, 147(9):4438-4444. DOI: 10.1210/en.2006-0414.
|
[45] |
PECORI GIRALDI F, AMBROGIO A G, ANDRIOLI M,et al. Potential role for retinoic acid in patients with Cushing's disease[J]. J Clin Endocrinol Metab, 2012, 97(10):3577-3583. DOI: 10.1210/jc.2012-2328.
|
[46] |
VILAR L, ALBUQUERQUE J L, LYRA R,et al. The role of isotretinoin therapy for Cushing's disease:results of a prospective study[J]. Int J Endocrinol, 2016, 2016:8173182. DOI: 10.1155/2016/8173182.
|
[47] |
ZHANG D, DU L, HEANEY A P. Testicular receptor-4:novel regulator of glucocorticoid resistance[J]. J Clin Endocrinol Metab, 2016, 101(8):3123-3133. DOI: 10.1210/jc.2016-1379.
|
[48] |
ZHANG D, BERGSNEIDER M, WANG M B,et al. Targeting the ERK pathway for the treatment of Cushing's disease[J]. Oncotarget, 2016, 7(43):69149-69158. DOI: 10.18632/oncotarget.12381.
|