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Journal articles on the topic 'Stanniocalcin-2'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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1

Luo, Ching-Wei, Margareta D. Pisarska, and Aaron J. W. Hsueh. "Identification of a Stanniocalcin Paralog, Stanniocalcin-2, in Fish and the Paracrine Actions of Stanniocalcin-2 in the Mammalian Ovary." Endocrinology 146, no. 1 (2005): 469–76. http://dx.doi.org/10.1210/en.2004-1197.

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2

Chang, A. C. M., and Roger R. Reddel. "Identification of a second stanniocalcin cDNA in mouse and human: Stanniocalcin 2." Molecular and Cellular Endocrinology 141, no. 1-2 (1998): 95–99. http://dx.doi.org/10.1016/s0303-7207(98)00097-5.

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3

Steffensen, Lasse B., Cheryl A. Conover, Martin M. Bjørklund, Thomas Ledet, Jacob F. Bentzon, and Claus Oxvig. "Stanniocalcin-2 overexpression reduces atherosclerosis in hypercholesterolemic mice." Atherosclerosis 248 (May 2016): 36–43. http://dx.doi.org/10.1016/j.atherosclerosis.2016.02.026.

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4

Zhou, Juan, Yinghua Li, Lina Yang, et al. "Stanniocalcin 2 improved osteoblast differentiation via phosphorylation of ERK." Molecular Medicine Reports 14, no. 6 (2016): 5653–59. http://dx.doi.org/10.3892/mmr.2016.5951.

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5

ZHANG, ZHEN-HAI, YA-GUANG WU, CHENG-KUN QIN, ZHONG-HOU RONG, ZHONG-XUE SU, and GUO-ZHE XIAN. "Stanniocalcin 2 expression predicts poor prognosis of hepatocellular carcinoma." Oncology Letters 8, no. 5 (2014): 2160–64. http://dx.doi.org/10.3892/ol.2014.2520.

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6

Sarapio, Elaine, Samir K. De Souza, Jorge F. A. Model, Marcia Trapp, and Roselis S. M. Da Silva. "Stanniocalcin-1 and -2 effects on glucose and lipid metabolism in white adipose tissue from fed and fasted rats." Canadian Journal of Physiology and Pharmacology 97, no. 10 (2019): 916–23. http://dx.doi.org/10.1139/cjpp-2019-0023.

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Stanniocalcin-1 and -2 belong to a family of molecules that exhibit both paracrine and autocrine effects in mammalian cells. Human stanniocalcin-1 (hSTC-1) is expressed in a wide range of tissues, including white adipose tissue. In fed rats, hSTC-1 increases carbon flux from glucose to lipids in retroperitoneal white adipose tissue. Human stanniocalcin-2 (hSTC-2) is expressed in almost all tissues and regulates various biological processes. The aim of this work was to study the action of hSTC-1 and hSTC-2 in the lipid and glucose metabolism of epididymal white adipose tissue (eWAT) in rats in

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7

Zhou, Han, Ying-Ying Li, Wei-Qiang Zhang, Dan Lin, Wei-Ming Zhang, and Wei-Da Dong. "Expression of Stanniocalcin-1 and Stanniocalcin-2 in Laryngeal Squamous Cell Carcinoma and Correlations with Clinical and Pathological Parameters." PLoS ONE 9, no. 4 (2014): e95466. http://dx.doi.org/10.1371/journal.pone.0095466.

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8

Hu, Lixia, Yanyan Zha, Fanliang Kong, and Yueyin Pan. "Prognostic value of high stanniocalcin 2 expression in solid cancers." Medicine 98, no. 43 (2019): e17432. http://dx.doi.org/10.1097/md.0000000000017432.

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9

Gagliardi, Anthony D., Evan Y. W. Kuo, Sanda Raulic, Graham F. Wagner, and Gabriel E. DiMattia. "Human stanniocalcin-2 exhibits potent growth-suppressive properties in transgenic mice independently of growth hormone and IGFs." American Journal of Physiology-Endocrinology and Metabolism 288, no. 1 (2005): E92—E105. http://dx.doi.org/10.1152/ajpendo.00268.2004.

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Stanniocalcin (STC)-2 was discovered by its primary amino acid sequence identity to the hormone STC-1. The function of STC-2 has not been examined; thus we generated two lines of transgenic mice overexpressing human (h)STC-2 to gain insight into its potential functions through identification of overt phenotypes. Analysis of mouse Stc2 gene expression indicates that, unlike Stc1, it is not highly expressed during development but exhibits overlapping expression with Stc1 in adult mice, with heart and skeletal muscle exhibiting highest steady-state levels of Stc2 mRNA. Constitutive overexpression

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10

Meyer, Hellmuth-A., Angelika Tölle, Monika Jung, et al. "Identification of Stanniocalcin 2 as Prognostic Marker in Renal Cell Carcinoma." European Urology 55, no. 3 (2009): 669–78. http://dx.doi.org/10.1016/j.eururo.2008.04.001.

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11

Zeiger, W., D. Ito, C. Swetlik, M. Oh-hora, M. L. Villereal, and G. Thinakaran. "Stanniocalcin 2 Is a Negative Modulator of Store-Operated Calcium Entry." Molecular and Cellular Biology 31, no. 18 (2011): 3710–22. http://dx.doi.org/10.1128/mcb.05140-11.

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12

Kim, Pyung-Hwan, Sang-Su Na, Bomnaerin Lee, Joo-Hyun Kim, and Je-Yoel Cho. "Stanniocalcin 2 enhances mesenchymal stem cell survival by suppressing oxidative stress." BMB Reports 48, no. 12 (2015): 702–7. http://dx.doi.org/10.5483/bmbrep.2015.48.12.158.

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13

Jiang, Shu-ting, Hua-qiao Wang, Tie-cheng Yang, et al. "Expression of Stanniocalcin 2 in Breast Cancer and Its Clinical Significance." Current Medical Science 39, no. 6 (2019): 978–83. http://dx.doi.org/10.1007/s11596-019-2131-2.

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14

Mittapalli, Venugopal Rao, Felicitas Pröls, Ruijin Huang, Bodo Christ, and Martin Scaal. "Avian stanniocalcin-2 is expressed in developing striated muscle and joints." Anatomy and Embryology 211, no. 5 (2006): 519–23. http://dx.doi.org/10.1007/s00429-006-0100-6.

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15

Wang, Yuxia, Ying Gao, Hairong Cheng, Guichun Yang, and Wenhua Tan. "Stanniocalcin 2 promotes cell proliferation and cisplatin resistance in cervical cancer." Biochemical and Biophysical Research Communications 466, no. 3 (2015): 362–68. http://dx.doi.org/10.1016/j.bbrc.2015.09.029.

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16

Flik, G., T. Labedz, J. A. Neelissen, R. G. Hanssen, S. E. Wendelaar Bonga, and P. K. Pang. "Rainbow trout corpuscles of Stannius: stanniocalcin synthesis in vitro." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 258, no. 5 (1990): R1157—R1164. http://dx.doi.org/10.1152/ajpregu.1990.258.5.r1157.

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In fresh-water rainbow trout, Oncorhynchus mykiss (formerly called Salmo gairdneri), experimentally induced mild hypercalcemia results in release of immunoreactive stanniocalcin from the corpuscles of Stannius (CS) and stimulated synthetic and releasing activities of the glands as measured in vitro. Pulse-chase experiments showed that stanniocalcin (STC) is a 56-kDa glycoprotein, processed from a 64-kDa precursor, prostanniocalcin (PSTC). PSTC and STC are homodimeric molecules that are readily split into monomers in the presence of reducing agents such as 2-mercaptoethanol. The monomeric form

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17

Lin, Shaojun, Qiaojuan Guo, Jiangmei Wen, et al. "Survival analyses correlate stanniocalcin 2 overexpression to poor prognosis of nasopharyngeal carcinomas." Journal of Experimental & Clinical Cancer Research 33, no. 1 (2014): 26. http://dx.doi.org/10.1186/1756-9966-33-26.

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18

Yokobori, Takehiko, Koshi Mimori, Hideshi Ishii, et al. "Clinical Significance of Stanniocalcin 2 as a Prognostic Marker in Gastric Cancer." Annals of Surgical Oncology 17, no. 10 (2010): 2601–7. http://dx.doi.org/10.1245/s10434-010-1086-0.

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19

JELLINEK, Derek A., Andy C. CHANG, Martin R. LARSEN, Xin WANG, Phillip J. ROBINSON, and Roger R. REDDEL. "Stanniocalcin 1 and 2 are secreted as phosphoproteins from human fibrosarcoma cells." Biochemical Journal 350, no. 2 (2000): 453. http://dx.doi.org/10.1042/0264-6021:3500453.

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20

JELLINEK, Derek A., Andy C. CHANG, Martin R. LARSEN, Xin WANG, Phillip J. ROBINSON, and Roger R. REDDEL. "Stanniocalcin 1 and 2 are secreted as phosphoproteins from human fibrosarcoma cells." Biochemical Journal 350, no. 2 (2000): 453–61. http://dx.doi.org/10.1042/bj3500453.

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Stanniocalcin 1 (STC1) and stanniocalcin 2 (STC2) are two recently identified mammalian peptide hormones. STC1 plays a role in calcium and phosphate homoeostasis, while the role of STC2 is unknown. We examined a human fibrosarcoma cell line, HT1080, that has high steady-state STC1 and STC2 mRNA levels, to determine whether these proteins are secreted. Following incubation of HT1080 cells with 32P, labelled STC1 and STC2 were found to be secreted into the medium. STC1 was phosphorylated in vitro by protein kinase C (PKC). In vitro and in vivo phosphorylation both occurred exclusively on serine

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21

Volland, Sonja, Wilfried Kugler, Lothar Schweigerer, Jörg Wilting, and Jürgen Becker. "Stanniocalcin 2 promotes invasion and is associated with metastatic stages in neuroblastoma." International Journal of Cancer 125, no. 9 (2009): 2049–57. http://dx.doi.org/10.1002/ijc.24564.

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22

Chang, Andy C. M., Jeff Hook, Frances A. Lemckert, et al. "The Murine Stanniocalcin 2 Gene Is a Negative Regulator of Postnatal Growth." Endocrinology 149, no. 5 (2008): 2403–10. http://dx.doi.org/10.1210/en.2007-1219.

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Stanniocalcin (STC), a secreted glycoprotein, was first studied in fish as a classical hormone with a role in regulating serum calcium levels. There are two closely related proteins in mammals, STC1 and STC2, with functions that are currently unclear. Both proteins are expressed in numerous mammalian tissues rather than being secreted from a specific endocrine gland. No phenotype has been detected yet in Stc1-null mice, and to investigate whether Stc2 could have compensated for the loss of Stc1, we have now generated Stc2−/− and Stc1−/−Stc2−/− mice. Although Stc1 is expressed in the ovary and

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23

Harper, Tod A., Aditya D. Joshi, and Cornelis J. Elferink. "Identification of Stanniocalcin 2 as a Novel Aryl Hydrocarbon Receptor Target Gene." Journal of Pharmacology and Experimental Therapeutics 344, no. 3 (2012): 579–88. http://dx.doi.org/10.1124/jpet.112.201111.

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24

Tamura, Kenji, Mutsuo Furihata, Su-Yong Chung, et al. "Stanniocalcin 2 overexpression in castration-resistant prostate cancer and aggressive prostate cancer." Cancer Science 100, no. 5 (2009): 914–19. http://dx.doi.org/10.1111/j.1349-7006.2009.01117.x.

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25

Xiao, Li-Juan, Jin-Xiang Yuan, Xin-Xin Song, Yin-Chuan Li, Zhao-Yuan Hu, and Yi-Xun Liu. "Expression and regulation of stanniocalcin 1 and 2 in rat uterus during embryo implantation and decidualization." Reproduction 131, no. 6 (2006): 1137–49. http://dx.doi.org/10.1530/rep.1.01100.

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Stanniocalcin-1 (STC-1) is a recently discovered polypeptide hormone, while stanniocalcin-2 (STC-2) is a subsequently identified homologue of stanniocalcin-1. Although previous studies have shown that both STC-1 and -2 are involved in various physiological processes, such as ion transport, reproduction and development, their expression in the uterus and roles in implantation and early pregnancy are unclear. Here we have investigated the expression and regulation of both STC-1 and STC-2 in rat uterus during early pregnancy under various physiological conditions. We show that only basal levels o

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26

Law, Alice Y. S., Keng P. Lai, Carman K. M. Ip, Alice S. T. Wong, Graham F. Wagner, and Chris K. C. Wong. "Epigenetic and HIF-1 regulation of stanniocalcin-2 expression in human cancer cells." Experimental Cell Research 314, no. 8 (2008): 1823–30. http://dx.doi.org/10.1016/j.yexcr.2008.03.001.

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27

Law, Alice Y., Richard L. Hébert, Rania Nasrallah, Robert Langenbach, Chris K. C. Wong, and Graham F. Wagner. "Cyclooxygenase-2 mediates induction of the renal stanniocalcin-1 gene by arginine vasopressin." Molecular and Cellular Endocrinology 381, no. 1-2 (2013): 210–19. http://dx.doi.org/10.1016/j.mce.2013.07.008.

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28

Coulson-Gilmer, Camilla, Matthew P. Humphries, Sreekumar Sundara Rajan, et al. "Stanniocalcin 2 expression is associated with a favourable outcome in male breast cancer." Journal of Pathology: Clinical Research 4, no. 4 (2018): 241–49. http://dx.doi.org/10.1002/cjp2.106.

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29

Yuan, Qiong, Lin Zhan, Li-Li Zhang, et al. "Stanniocalcin 2 induces oxaliplatin resistance in colorectal cancer cells by upregulating P-glycoprotein." Canadian Journal of Physiology and Pharmacology 94, no. 9 (2016): 929–35. http://dx.doi.org/10.1139/cjpp-2015-0530.

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Multidrug resistance (MDR) limits the anticancer effects of chemotherapy in patients with metastatic colorectal cancer (CRC). Oxaliplatin is a common component of combinational therapeutic regimens administered to patients with metastatic CRC; however, it is also used as a constituent of adjuvant therapy for patients at a risk of recurrent disease. In the present study, we investigated the role of stanniocalcin 2 (STC2) in chemoresistance. STC2 knockdown sensitized chemoresistant CRC cells to oxaliplatin. Moreover, the expression of exogenous STC2 in chemonaïve CRC cells induced oxaliplatin re

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30

Yahata, Kensei, Kiyoshi Mori, Masashi Mukoyama, et al. "Regulation of stanniocalcin 1 and 2 expression in the kidney by klotho gene." Biochemical and Biophysical Research Communications 310, no. 1 (2003): 128–34. http://dx.doi.org/10.1016/j.bbrc.2003.08.131.

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31

Frystyk, Jan, Enrique Teran, Mette Faurholdt Gude, Mette Bjerre, and Rikke Hjortebjerg. "Pregnancy-associated plasma proteins and Stanniocalcin-2 – Novel players controlling IGF-I physiology." Growth Hormone & IGF Research 53-54 (August 2020): 101330. http://dx.doi.org/10.1016/j.ghir.2020.101330.

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32

Paciga, Mark, Kathi James, J. Ryan J. Gillespie, and Graham F. Wagner. "Evidence for cross-talk between stanniocalcins." Canadian Journal of Physiology and Pharmacology 83, no. 11 (2005): 953–56. http://dx.doi.org/10.1139/y05-055.

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There are 2 forms of stanniocalcin (STC) produced by the STC-1 gene; a 50 kDa polypeptide known as STC50 and a recently discovered group of higher molecular weight variants that are collectively referred to as big STC. Both have different tissue patterns of expression and different intracellular targeting pathways. STC50 functions locally in tissues such as muscle, liver, and kidney and is targeted to mitochondria. Big STC, on the other hand, is made by the ovaries. It signals both locally on nearby corpus luteal cells and systemically. Interestingly, however, receptor binding assays employing

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33

Law, Alice Y. S., and Chris K. C. Wong. "Stanniocalcin-2 is a HIF-1 target gene that promotes cell proliferation in hypoxia." Experimental Cell Research 316, no. 3 (2010): 466–76. http://dx.doi.org/10.1016/j.yexcr.2009.09.018.

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34

Law, Alice Y. S., and Chris K. C. Wong. "Stanniocalcin-2 promotes epithelial–mesenchymal transition and invasiveness in hypoxic human ovarian cancer cells." Experimental Cell Research 316, no. 20 (2010): 3425–34. http://dx.doi.org/10.1016/j.yexcr.2010.06.026.

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35

Staehler, Michael. "Editorial Comment on: Identification of Stanniocalcin 2 as Prognostic Marker in Renal Cell Carcinoma." European Urology 55, no. 3 (2009): 678. http://dx.doi.org/10.1016/j.eururo.2008.04.002.

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36

Na, Sang-su, Mark Borris Aldonza, Hye-Jin Sung, et al. "Stanniocalcin-2 (STC2): A potential lung cancer biomarker promotes lung cancer metastasis and progression." Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics 1854, no. 6 (2015): 668–76. http://dx.doi.org/10.1016/j.bbapap.2014.11.002.

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37

Byun, Jong-Seon, Jae-Won Lee, Su Young Kim, et al. "Neuroprotective effects of stanniocalcin 2 following kainic acid-induced hippocampal degeneration in ICR mice." Peptides 31, no. 11 (2010): 2094–99. http://dx.doi.org/10.1016/j.peptides.2010.08.002.

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38

Moore, E., R. Kuestner, D. Conklin, et al. "Stanniocalcin 2: Characterization of the Protein and its Localization to Human Pancreatic Alpha Cells." Hormone and Metabolic Research 31, no. 07 (1999): 406–14. http://dx.doi.org/10.1055/s-2007-978764.

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39

Panagiotou, Grigorios, Athanasios D. Anastasilakis, Georgios Kynigopoulos, et al. "Physiological parameters regulating circulating levels of the IGFBP-4/Stanniocalcin-2/PAPP-A axis." Metabolism 75 (October 2017): 16–24. http://dx.doi.org/10.1016/j.metabol.2017.07.003.

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40

Li, Ji-Bin, Zhe-Xian Liu, Rui Zhang, et al. "Sp1 contributes to overexpression of stanniocalcin 2 through regulation of promoter activity in colon adenocarcinoma." World Journal of Gastroenterology 25, no. 22 (2019): 2776–87. http://dx.doi.org/10.3748/wjg.v25.i22.2776.

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41

He, Huocong, Shuo Qie, Qiaojuan Guo, et al. "Stanniocalcin 2 (STC2) expression promotes post-radiation survival, migration and invasion of nasopharyngeal carcinoma cells." Cancer Management and Research Volume 11 (July 2019): 6411–24. http://dx.doi.org/10.2147/cmar.s197607.

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42

ARIGAMI, TAKAAKI, YOSHIKAZU UENOSONO, SUMIYA ISHIGAMI, et al. "Clinical significance of stanniocalcin 2 expression as a predictor of tumor progression in gastric cancer." Oncology Reports 30, no. 6 (2013): 2838–44. http://dx.doi.org/10.3892/or.2013.2775.

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43

Ferreira do Carmo, Andreia, Mauricio Rocha Dourado, Carine Ervolino de Oliveira, et al. "Stanniocalcin 2 contributes to aggressiveness and is a prognostic marker for oral squamous cell carcinoma." Experimental Cell Research 393, no. 2 (2020): 112092. http://dx.doi.org/10.1016/j.yexcr.2020.112092.

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44

Jepsen, Malene R., Søren Kløverpris, Jakob H. Mikkelsen, et al. "Stanniocalcin-2 Inhibits Mammalian Growth by Proteolytic Inhibition of the Insulin-like Growth Factor Axis." Journal of Biological Chemistry 290, no. 6 (2014): 3430–39. http://dx.doi.org/10.1074/jbc.m114.611665.

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45

Fazio, Elena N., Gabriel E. DiMattia, Sami A. Chadi, Kristin D. Kernohan, and Christopher L. Pin. "Stanniocalcin 2 alters PERK signalling and reduces cellular injury during cerulein induced pancreatitis in mice." BMC Cell Biology 12, no. 1 (2011): 17. http://dx.doi.org/10.1186/1471-2121-12-17.

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46

Feng, Linsen, Jianhua Ma, Haiming Ji, Yichun Liu, and Weixing Hu. "MiR-184 Retarded the Proliferation, Invasiveness and Migration of Glioblastoma Cells by Repressing Stanniocalcin-2." Pathology & Oncology Research 24, no. 4 (2017): 853–60. http://dx.doi.org/10.1007/s12253-017-0298-z.

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47

Aydin, Hulya Ayik, Tayfun Toptas, Selen Bozkurt, et al. "Stanniocalcin-2 May Be a Potentially Valuable Prognostic Marker in Endometrial Cancer: a Preliminary Study." Pathology & Oncology Research 25, no. 2 (2019): 751–57. http://dx.doi.org/10.1007/s12253-018-00576-y.

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48

Joshi, Aditya D., Ekram Hossain, and Cornelis J. Elferink. "Epigenetic Regulation by Agonist-Specific Aryl Hydrocarbon Receptor Recruitment of Metastasis-Associated Protein 2 Selectively Induces Stanniocalcin 2 Expression." Molecular Pharmacology 92, no. 3 (2017): 366–74. http://dx.doi.org/10.1124/mol.117.108878.

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49

He, Huocong, Shuo Qie, Qiaojuan Guo, et al. "Stanniocalcin 2 (STC2) Expression Promotes Post-Radiation Survival, Migration and Invasion of Nasopharyngeal Carcinoma Cells [Corrigendum]." Cancer Management and Research Volume 11 (December 2019): 10409–10. http://dx.doi.org/10.2147/cmar.s240959.

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50

Wang, Jian, Sana Sahengbieke, Xiaoping Xu, et al. "Gene expression analyses identify a relationship between stanniocalcin 2 and the malignant behavior of colorectal cancer." OncoTargets and Therapy Volume 11 (October 2018): 7155–68. http://dx.doi.org/10.2147/ott.s167780.

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