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Journal articles on the topic 'GRIM-19'

Author: Grafiati

Published: 4 September 2021

Last updated: 29 July 2025

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1

Yang, Yang, Yanyan Sun, Laiyang Cheng, et al. "GRIM-19, a gene associated with retinoid-interferon-induced mortality, affects endometrial receptivity and embryo implantation." Reproduction, Fertility and Development 29, no. 7 (2017): 1447. http://dx.doi.org/10.1071/rd16104.

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GRIM-19 is associated with apoptosis, abnormal proliferation, immune tolerance and malignant transformation, and it also plays an important role in early embryonic development. Although the homologous deletion of GRIM-19 causes embryonic lethality in mice, the precise role of GRIM-19 in embryo implantation has not been elucidated. Here we show that GRIM-19 plays an important role in endometrial receptivity and embryo implantation. Day 1 to Day 6 pregnant mouse uteri were collected. Immunohistochemistry studies revealed the presence of GRIM-19 on the luminal epithelium and glandular epithelium

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2

Cheng, Yong, Hong-yan Zhang, Ying Zhou, Feng Tao, and Yong-hua Yu. "Decreased expression of GRIM-19 and its association with high-risk HPV infection in cervical squamous intraepithelial neoplasias and cancer." Clinical & Investigative Medicine 37, no. 2 (2014): 77. http://dx.doi.org/10.25011/cim.v37i2.21089.

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Purpose: GRIM-19 has been shown to be down-regulated in cervical cancers. This study investigated the expression of GRIM-19 in cervical intra-epithelial neoplasias and its association with high-risk human papillomavirus (HR-HPV) infection. Methods: The expression of GRIM-19 was assessed in cervical exfoliated cells and cervical intra-epithelial neoplasia tissues by immunohistochemistry, and the level of GRIM-19 was also evaluated by Western blotting using cervical exfoliated cells. HR-HPV infection of cervical exfoliated cells was detected by HC II. Results: GRIM-19 is predominantly expressed

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3

Huang, Guochang, Hao Lu, Aijun Hao, et al. "GRIM-19, a Cell Death Regulatory Protein, Is Essential for Assembly and Function of Mitochondrial Complex I." Molecular and Cellular Biology 24, no. 19 (2004): 8447–56. http://dx.doi.org/10.1128/mcb.24.19.8447-8456.2004.

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ABSTRACT Mitochondria play essential roles in cellular energy production via the oxidative phosphorylation system (OXPHOS) consisting of five multiprotein complexes and also in the initiation of apoptosis. NADH:ubiquinone oxidoreductase (complex I) is the largest complex that catalyzes the first step of electron transfer in the OXPHOS system. GRIM-19 was originally identified as a nuclear protein with apoptotic nature in interferon (IFN)- and all-trans-retinoic acid (RA)-induced tumor cells. To reveal its biological role, we generated mice deficient in GRIM-19 by gene targeting. Homologous del

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4

Moon, Young-Mee, Jennifer Lee, Seon-Yeong Lee, et al. "Gene-associated retinoid-interferon-induced mortality 19 (GRIM-19) attenuates autoimmune arthritis by regulation of Th17 and Treg cells (VAC3P.957)." Journal of Immunology 192, no. 1_Supplement (2014): 73.19. http://dx.doi.org/10.4049/jimmunol.192.supp.73.19.

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Abstract Signal transducer and activator of transcription 3 (STAT3) is a key transcriptional factor in interleukin (IL)-6-mediated Th17 differentiation. Because Th17 is believed to be a central player in rheumatoid arthritis (RA), we hypothesized that an endogenous STAT3 inhibitor, genes associated with retinoid-interferon-induced mortality 19 (GRIM-19), could attenuate collagen-induced arthritis (CIA) by suppressing Th17 and reciprocally increasing Treg. The numbers of CD4+/IL-17+ cells and CD4+ phosphorylated (p)-STAT3+ cells were decreased, while the numbers of CD4+/CD25+/Foxp3+ cells and C

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5

Kummari, Raghupathi, Shubhankar Dutta, Shubhangi Patil, Snehal Pandav Mudrale, and Kakoli Bose. "Elucidating the role of GRIM-19 as a substrate and allosteric activator of pro-apoptotic serine protease HtrA2." Biochemical Journal 478, no. 6 (2021): 1241–59. http://dx.doi.org/10.1042/bcj20200923.

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HtrA2 (high-temperature requirement A2) and GRIM-19 (gene associated with retinoic and interferon-induced mortality 19 protein) are involved in various biological functions with their deregulation leading to multiple diseases. Although it is known that the interaction between GRIM-19 with HtrA2 promotes the pro-apoptotic activity of the latter, the mechanistic details remained elusive till date. Moreover, designing allosteric modulators of HtrA2 remains obscure due to lack of adequate information on the mode of interaction with its natural substrates cum binding partners. Therefore, in this st

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6

Máximo, Valdemar, Jorge Lima, Paula Soares, André Silva, Inês Bento, and Manuel Sobrinho-Simões. "GRIM-19 in Health and Disease." Advances in Anatomic Pathology 15, no. 1 (2008): 46–53. http://dx.doi.org/10.1097/pap.0b013e31815e5258.

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7

Moreira, Severina, Marcelo Correia, Paula Soares, and Valdemar Máximo. "GRIM-19 function in cancer development." Mitochondrion 11, no. 5 (2011): 693–99. http://dx.doi.org/10.1016/j.mito.2011.05.011.

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8

Papa, F., M. Delia, R. Trentadue, et al. "Differential Effects of All-Trans Retinoic Acid on the Growth of Human Keratinocytes and Mouth Carcinoma Epidermoid Cultures. Involvement of GRIM-19 and Complex I of the Respiratory Chain." International Journal of Immunopathology and Pharmacology 20, no. 4 (2007): 719–29. http://dx.doi.org/10.1177/039463200702000407.

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Squamous cell carcinoma (SSC) is the most frequent malignant tumor of the oral cavity. A study on the effect of all-trans retinoic acid (RA) on cell growth, expression of GRIM-19 and content and activity of complex I of the mitochondrial respiratory chain in normal human keratinocytes (NHEK) and mouth carcinoma cells with low (HN) and high (KB) transformation grade was carried out. In NHEK cells, RA treatment resulted in growth suppression, significant overexpression of GRIM-19 protein, enhanced content of complex I but depressed activity of NADH-UQ oxidoreductase activity of the complex. In H

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9

Chen, Yong, Wai Hong Yuen, Jianlin Fu, et al. "The Mitochondrial Respiratory Chain Controls Intracellular Calcium Signaling and NFAT Activity Essential for Heart Formation in Xenopus laevis." Molecular and Cellular Biology 27, no. 18 (2007): 6420–32. http://dx.doi.org/10.1128/mcb.01946-06.

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ABSTRACT The mitochondrial respiratory chain (MRC) plays crucial roles in cellular energy production. However, its function in early embryonic development remains largely unknown. To address this issue, GRIM-19, a newly identified MRC complex I subunit, was knocked down in Xenopus laevis embryos. A severe deficiency in heart formation was observed, and the deficiency could be rescued by reintroducing human GRIM-19 mRNA. The mechanism involved was further investigated. We found that the activity of NFAT, a transcription factor family that contributes to early organ development, was downregulate

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10

Lu, Hao, and Xinmin Cao. "GRIM-19 Is Essential for Maintenance of Mitochondrial Membrane Potential." Molecular Biology of the Cell 19, no. 5 (2008): 1893–902. http://dx.doi.org/10.1091/mbc.e07-07-0683.

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GRIM-19 was found to copurify with complex I of mitochondrial respiratory chain and subsequently was demonstrated to be involved in complex I assembly and activity. To further understand its function in complex I, we dissected its functional domains by generating a number of deletion, truncation, and point mutants. The mitochondrial localization sequences were located at the N-terminus. Strikingly, deletion of residues 70–80, 90–100, or the whole C-terminal region (70–144) led to a loss of mitochondrial transmembrane potential (ΔΨm). However, similar deletions of another two complex I subunits

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11

Jin, Yong-Hao, Shin Jung, Shu-Guang Jin, Tae-Young Jung, Kyung-Sub Moon, and In-Young Kim. "GRIM-19 Expression and Function in Human Gliomas." Journal of Korean Neurosurgical Society 48, no. 1 (2010): 20. http://dx.doi.org/10.3340/jkns.2010.48.1.20.

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12

Qidwai, Waris, Salman Tariq, and Naveen Tariq. "COVID-19 in Pakistan : A Grim - Looking Trajectory." World Family Medicine Journal/Middle East Journal of Family Medicine 18, no. 7 (2020): 43–49. http://dx.doi.org/10.5742/mewfm.2020.93834.

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13

Zhao, Yan-Da, Fei-Fei Li, Wan-Hua Ren, and Cheng-Yong Qin. "Clinical significance of GRIM-19 expression in hepatocellular carcinoma." World Chinese Journal of Digestology 19, no. 20 (2011): 2123. http://dx.doi.org/10.11569/wcjd.v19.i20.2123.

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14

Pang, Li, Yan Xia, Dawei Wang, and Xiangwei Meng. "Antitumor activity of iNGR-GRIM-19 in colorectal cancer." Japanese Journal of Clinical Oncology 47, no. 9 (2017): 795–808. http://dx.doi.org/10.1093/jjco/hyx090.

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15

Kalvakolanu, Dhan V., Sudhakar Kalakonda, Shreeram C. Nallar, and Peng Sun. "203 GRIM-19: A novel cytokine-induced tumor suppressor." Cytokine 43, no. 3 (2008): 287–88. http://dx.doi.org/10.1016/j.cyto.2008.07.266.

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16

Ferreira, António Carlos, Lígia Gomes, Valdemar Máximo та ін. "GRIM-19 mutations are not associated with Crohnʼs disease". Inflammatory Bowel Diseases 14, № 3 (2008): 434–35. http://dx.doi.org/10.1002/ibd.20313.

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17

Arora, Suraj, Vishakha Grover, Priyanka Saluja, et al. "Literature Review of Omicron: A Grim Reality Amidst COVID-19." Microorganisms 10, no. 2 (2022): 451. http://dx.doi.org/10.3390/microorganisms10020451.

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Coronavirus disease 2019 (COVID-19) first emerged in Wuhan city in December 2019, and became a grave global concern due to its highly infectious nature. The Severe Acute Respiratory Coronavirus-2, with its predecessors (i.e., MERS-CoV and SARS-CoV) belong to the family of Coronaviridae. Reportedly, COVID-19 has infected 344,710,576 people around the globe and killed nearly 5,598,511 persons in the short span of two years. On November 24, 2021, B.1.1.529 strain, later named Omicron, was classified as a Variant of Concern (VOC). SARS-CoV-2 has continuously undergone a series of unprecedented mut

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18

Kalakonda, S., S. C. Nallar, D. J. Lindner, et al. "GRIM-19 mutations fail to inhibit v-Src-induced oncogenesis." Oncogene 33, no. 24 (2013): 3195–204. http://dx.doi.org/10.1038/onc.2013.271.

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19

Hwang, Sun-Nyoung, Jae-Cheon Kim, and Seong Yun Kim. "Heterogeneity of GRIM-19 Expression in the Adult Mouse Brain." Cellular and Molecular Neurobiology 39, no. 7 (2019): 935–51. http://dx.doi.org/10.1007/s10571-019-00689-1.

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20

Fan, Xiao-Yun, Zi-Feng Jiang, Li Cai, and Rong-Yu Liu. "Expression and clinical significance of GRIM-19 in lung cancer." Medical Oncology 29, no. 5 (2012): 3183–89. http://dx.doi.org/10.1007/s12032-012-0249-1.

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21

Chen, Honglei, Xiaohui Deng, Yang Yang, et al. "Expression of GRIM-19 in missed abortion and possible pathogenesis." Fertility and Sterility 103, no. 1 (2015): 138–46. http://dx.doi.org/10.1016/j.fertnstert.2014.10.012.

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22

Zhou, Ying, Fei Xu, Feng Tao, et al. "GRIM-19 Restores Cervical Cancer Cell Senescence by Repressing hTERT Transcription." Journal of Interferon & Cytokine Research 36, no. 8 (2016): 506–15. http://dx.doi.org/10.1089/jir.2015.0125.

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23

He, Xuelian, and Xinmin Cao. "Identification of alternatively spliced GRIM-19 mRNA in kidney cancer tissues." Journal of Human Genetics 55, no. 8 (2010): 507–11. http://dx.doi.org/10.1038/jhg.2010.57.

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24

Kalakonda, S., S. C. Nallar, S. Jaber, et al. "Monoallelic loss of tumor suppressor GRIM-19 promotes tumorigenesis in mice." Proceedings of the National Academy of Sciences 110, no. 45 (2013): E4213—E4222. http://dx.doi.org/10.1073/pnas.1303760110.

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25

Liu, Qian, Lulu Wang, Zhaojuan Wang та ін. "GRIM-19 opposes reprogramming of glioblastoma cell metabolism via HIF1α destabilization". Carcinogenesis 34, № 8 (2013): 1728–36. http://dx.doi.org/10.1093/carcin/bgt125.

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26

Kalvakolanu, Dhan V., Shreram C. Nallar, Peng Sun, and Sudhakar Kalakonda. "GRIM-19: A novel growth regulator that inhibits STAT3 and beyond." Cytokine 48, no. 1-2 (2009): 7. http://dx.doi.org/10.1016/j.cyto.2009.07.031.

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27

Hao, Miao, Zhenbo Shu, Hongyan Sun, et al. "GRIM-19 expression is a potent prognostic marker in colorectal cancer." Human Pathology 46, no. 12 (2015): 1815–20. http://dx.doi.org/10.1016/j.humpath.2015.07.020.

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28

Yeo, W. M., Yuji Isegawa, and Vincent T. K. Chow. "The U95 Protein of Human Herpesvirus 6B Interacts with Human GRIM-19: Silencing of U95 Expression Reduces Viral Load and Abrogates Loss of Mitochondrial Membrane Potential." Journal of Virology 82, no. 2 (2007): 1011–20. http://dx.doi.org/10.1128/jvi.01156-07.

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ABSTRACT To better understand the pathogenesis of human herpesvirus 6 (HHV-6), it is important to elucidate the functional aspects of immediate-early (IE) genes at the initial phase of the infection. To study the functional role of the HHV-6B IE gene encoding U95, we generated a U95-Myc fusion protein and screened a pretransformed bone marrow cDNA library for U95-interacting proteins, using yeast-two hybrid analysis. The most frequently appearing U95-interacting protein identified was GRIM-19, which belongs to the family of genes associated with retinoid-interferon mortality and serves as an e

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29

Zhang, Yanmin, Hongbo Hao, Shidou Zhao, et al. "Downregulation of GRIM-19 promotes growth and migration of human glioma cells." Cancer Science 102, no. 11 (2011): 1991–99. http://dx.doi.org/10.1111/j.1349-7006.2011.02059.x.

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30

Ma, X., S. Kalakonda, S. M. Srinivasula, S. P. Reddy, L. C. Platanias, and D. V. Kalvakolanu. "GRIM-19 associates with the serine protease HtrA2 for promoting cell death." Oncogene 26, no. 33 (2007): 4842–49. http://dx.doi.org/10.1038/sj.onc.1210287.

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31

Lin, Haili, Tianqi Lin, Jiangui Lin, et al. "Inhibition of miR-423-5p suppressed prostate cancer through targeting GRIM-19." Gene 688 (March 2019): 93–97. http://dx.doi.org/10.1016/j.gene.2018.11.021.

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32

Wang, Jing, Xiaohui Deng, Yang Yang, Xingsheng Yang, Beihua Kong, and Lan Chao. "Expression of GRIM-19 in adenomyosis and its possible role in pathogenesis." Fertility and Sterility 105, no. 4 (2016): 1093–101. http://dx.doi.org/10.1016/j.fertnstert.2015.12.019.

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33

Blanc-Durand, Félix, Geraldine M. Camilleri, Arnaud Bayle, et al. "Clinical Utility of Comprehensive Liquid Molecular Profiling in Patients With Advanced Endometrial Cancer." Obstetrical & Gynecological Survey 80, no. 2 (2025): 91–93. https://doi.org/10.1097/01.ogx.0001108092.35846.d7.

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(Abstracted from Cancer 2024;130(19):3311–3320) Endometrial cancer (EC) has been increasing in incidence and mortality rates due to increased prevalence of risk factors such as obesity, metabolic syndrome, and diabetes. Many cases are treatable through a combination of methods, but up to 20% of cases are detected at an advanced stage, which has a grim prognosis.

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34

Nepal, Richa, and Bharosha Bhattarai. "The Grim Reality of Health System Uncovered with COVID-19 Pandemic in Nepal." Journal of Nepal Health Research Council 18, no. 3 (2020): 569–71. http://dx.doi.org/10.33314/jnhrc.v18i3.2755.

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With advent of community transmission of COVID-19 in Nepal, the number of cases continues to rise and poses threat to the fragile health system of our country. ‘Trace, isolate, test and treat’ is the strategy advocated by World Health Organization to fight against COVID-19. Despite the efforts for last nine months, Nepal lacks in some aspect of this strategy. Lack of prompt testing facilities and substandard quarantine and isolation centers, have led to mismanagement of cases. The panic regarding COVID-19, lack of adequate protective measures to healthcare workers in early stage of the pandemi

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35

Oniang'o, Ruth. "Rural Outreach Africa during COVID-19: Reaching those who fall through the CRACKS." African Journal of Food, Agriculture, Nutrition and Development 20, no. 6 (2020): 1. http://dx.doi.org/10.18697/ajfand.94.ed090.

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Here we go again. Just when we thought we could reopen the economy and even send children back to school, we see a resurgence in COVID-19 numbers. There are still too many challenges. Economies are on their knees, and yet grim as it looks, one sees opportunities. If these lockdowns resume, fragile economies will sink to levels never seen before in recent times and probably most difficult to recover from.

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36

Sun, P., S. C. Nallar, S. Kalakonda, D. J. Lindner, S. S. Martin, and D. V. Kalvakolanu. "GRIM-19 inhibits v-Src-induced cell motility by interfering with cytoskeletal restructuring." Oncogene 28, no. 10 (2009): 1339–47. http://dx.doi.org/10.1038/onc.2008.480.

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37

Lufei, C. "GRIM-19, a death-regulatory gene product, suppresses Stat3 activity via functional interaction." EMBO Journal 22, no. 6 (2003): 1325–35. http://dx.doi.org/10.1093/emboj/cdg135.

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38

Ekchariyawat, Peeraya, Arunee Thitithanyanont, Stitaya Sirisinha, and Pongsak Utaisincharoen. "Involvement of GRIM-19 in apoptosis induced in H5N1 virus-infected human macrophages." Innate Immunity 19, no. 6 (2013): 655–62. http://dx.doi.org/10.1177/1753425913479149.

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39

Dong, Du-Juan, Peng-Cheng Liu, Jin-Xing Wang, and Xiao-Fan Zhao. "The knockdown of Ha-GRIM-19 by RNA interference induced programmed cell death." Amino Acids 42, no. 4 (2010): 1297–307. http://dx.doi.org/10.1007/s00726-010-0824-8.

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40

Zhou, Tao, Lan Chao, Guohua Rong, Chenggang Wang, Rong Ma, and Xiao Wang. "Down-regulation of GRIM-19 is associated with STAT3 overexpression in breast carcinomas." Human Pathology 44, no. 9 (2013): 1773–79. http://dx.doi.org/10.1016/j.humpath.2012.12.018.

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41

Peng, Ting, Mei-mei Gu, Chang-sheng Zhao, et al. "The GRIM-19 plays a vital role in shrimps' responses to Vibrio alginolyticus." Fish & Shellfish Immunology 49 (February 2016): 34–44. http://dx.doi.org/10.1016/j.fsi.2015.12.016.

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42

Chen, Wanhong, Qingbai Liu, Bin Fu, Kai Liu, and Wenchao Jiang. "Overexpression of GRIM-19 accelerates radiation-induced osteosarcoma cells apoptosis by p53 stabilization." Life Sciences 208 (September 2018): 232–38. http://dx.doi.org/10.1016/j.lfs.2018.07.015.

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43

Sun, Peng, Shreeram C. Nallar, Abhijit Raha, et al. "GRIM-19 and p16INK4aSynergistically Regulate Cell Cycle Progression and E2F1-responsive Gene Expression." Journal of Biological Chemistry 285, no. 36 (2010): 27545–52. http://dx.doi.org/10.1074/jbc.m110.105767.

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44

Kalakonda, Sudhakar, Shreeram Nallar, and Dhan V. Kalvakolanu. "PS3-76 Study of the effect of GRIM-19 mutations on cell growth." Cytokine 52, no. 1-2 (2010): 97. http://dx.doi.org/10.1016/j.cyto.2010.07.415.

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45

Kapoor, Shailendra. "Grim-19 expression and its close association with tumor progression in systemic malignancies." Gene 517, no. 2 (2013): 240. http://dx.doi.org/10.1016/j.gene.2013.01.012.

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46

Fahmy, Khaled. "Egypt’s Old Affliction of Aloof Rulers." Current History 119, no. 821 (2020): 362–64. http://dx.doi.org/10.1525/curh.2020.119.821.362.

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Although official data suggest that Egypt avoided the worst of the COVID-19 pandemic, doctors have warned that the reality is far more grim. Their attempts to speak out have been met with harsh repression. A glance back at Egyptian history from the origins of the modern nation in the early nineteenth century reveals a consistent disregard for citizens’ health, apart from their usefulness as military conscripts.

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47

Chu, Dinh-Toi, Hue Vu Thi, Jaffar A. Al-Tawfiq, and Ziad A. Memish. "Children orphaned by COVID-19: A grim picture and the need of urgent actions." Travel Medicine and Infectious Disease 50 (November 2022): 102446. http://dx.doi.org/10.1016/j.tmaid.2022.102446.

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48

ZHANG, WEI, YE DU, TONG JIANG, WEI GENG, JIULI YUAN, and DUO ZHANG. "Upregulation of GRIM-19 inhibits the growth and invasion of human breast cancer cells." Molecular Medicine Reports 12, no. 2 (2015): 2919–25. http://dx.doi.org/10.3892/mmr.2015.3757.

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49

Chen, Yong, Hao Lu, Qian Liu, et al. "Function of GRIM-19, a Mitochondrial Respiratory Chain Complex I Protein, in Innate Immunity." Journal of Biological Chemistry 287, no. 32 (2012): 27227–35. http://dx.doi.org/10.1074/jbc.m112.340315.

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50

Shulga, Nataly, and John G. Pastorino. "GRIM-19-mediated translocation of STAT3 to mitochondria is necessary for TNF-induced necroptosis." Journal of Cell Science 125, no. 12 (2012): 2995–3003. http://dx.doi.org/10.1242/jcs.103093.

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