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Showing 1 to 12 of 202 entries
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Lentivirus-mediated RNA interference targeting UbcH10 reduces cell growth and invasion of human osteosarcoma cells via inhibition of Ki-67 and matrix metalloproteinases.

Oncology letters

Wang ST, Li DZ, Li JM, Fang J, Li HZ, Tong PJ, Liu FC.
PMID: 26137034
Oncol Lett. 2015 May;9(5):2171-2176. doi: 10.3892/ol.2015.3023. Epub 2015 Mar 10.

Osteosarcoma (OS) is the most commonly diagnosed primary malignancy affecting the bone. UbcH10 is a cancer-related E2-ubiquitin-conjugating enzyme. An overexpression of UbcH10 is significantly associated with tumor grade and cellular proliferation. However, limited evidence exists with regard to the...

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Wang ST, Li DZ, Li JM, et al. Lentivirus-mediated RNA interference targeting UbcH10 reduces cell growth and invasion of human osteosarcoma cells via inhibition of Ki-67 and matrix metalloproteinases. Oncol Lett. 2015;9(5):2171-2176doi: 10.3892/ol.2015.3023.
Wang, S. T., Li, D. Z., Li, J. M., Fang, J., Li, H. Z., Tong, P. J., & Liu, F. C. (2015). Lentivirus-mediated RNA interference targeting UbcH10 reduces cell growth and invasion of human osteosarcoma cells via inhibition of Ki-67 and matrix metalloproteinases. Oncology letters, 9(5), 2171-2176. https://doi.org/10.3892/ol.2015.3023
Wang, Shan-Tao, et al. "Lentivirus-mediated RNA interference targeting UbcH10 reduces cell growth and invasion of human osteosarcoma cells via inhibition of Ki-67 and matrix metalloproteinases." Oncology letters vol. 9,5 (2015): 2171-2176. doi: https://doi.org/10.3892/ol.2015.3023
Wang ST, Li DZ, Li JM, Fang J, Li HZ, Tong PJ, Liu FC. Lentivirus-mediated RNA interference targeting UbcH10 reduces cell growth and invasion of human osteosarcoma cells via inhibition of Ki-67 and matrix metalloproteinases. Oncol Lett. 2015 May;9(5):2171-2176. doi: 10.3892/ol.2015.3023. Epub 2015 Mar 10. PMID: 26137034; PMCID: PMC4467328.
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Apigenin Regulates Interleukin-1β-Induced Production of Matrix Metalloproteinase Both in the Knee Joint of Rat and in Primary Cultured Articular Chondrocytes.

Biomolecules & therapeutics

Park JS, Kim DK, Shin HD, Lee HJ, Jo HS, Jeong JH, Choi YL, Lee CJ, Hwang SC.
PMID: 26902085
Biomol Ther (Seoul). 2016 Mar 01;24(2):163-70. doi: 10.4062/biomolther.2015.217.

We examined whether apigenin affects the gene expression, secretion and activity of matrix metalloproteinase-3 (MMP-3) in primary cultured rabbit articular chondrocytes, as well as in vivo production of MMP-3 in the knee joint of rat to evaluate the potential...

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Park JS, Kim DK, Shin HD, et al. Apigenin Regulates Interleukin-1β-Induced Production of Matrix Metalloproteinase Both in the Knee Joint of Rat and in Primary Cultured Articular Chondrocytes. Biomol Ther (Seoul). 2016;24(2):163-70doi: 10.4062/biomolther.2015.217.
Park, J. S., Kim, D. K., Shin, H. D., Lee, H. J., Jo, H. S., Jeong, J. H., Choi, Y. L., Lee, C. J., & Hwang, S. C. (2016). Apigenin Regulates Interleukin-1β-Induced Production of Matrix Metalloproteinase Both in the Knee Joint of Rat and in Primary Cultured Articular Chondrocytes. Biomolecules & therapeutics, 24(2), 163-70. https://doi.org/10.4062/biomolther.2015.217
Park, Jin Sung, et al. "Apigenin Regulates Interleukin-1β-Induced Production of Matrix Metalloproteinase Both in the Knee Joint of Rat and in Primary Cultured Articular Chondrocytes." Biomolecules & therapeutics vol. 24,2 (2016): 163-70. doi: https://doi.org/10.4062/biomolther.2015.217
Park JS, Kim DK, Shin HD, Lee HJ, Jo HS, Jeong JH, Choi YL, Lee CJ, Hwang SC. Apigenin Regulates Interleukin-1β-Induced Production of Matrix Metalloproteinase Both in the Knee Joint of Rat and in Primary Cultured Articular Chondrocytes. Biomol Ther (Seoul). 2016 Mar 01;24(2):163-70. doi: 10.4062/biomolther.2015.217. PMID: 26902085; PMCID: PMC4774497.
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Combination of ciclopirox olamine and sphingosine-1-phosphate as granulation enhancer in diabetic wounds.

Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society

Lim NS, Sham A, Chee SM, Chan C, Raghunath M.
PMID: 27402256
Wound Repair Regen. 2016 Sep;24(5):795-809. doi: 10.1111/wrr.12463. Epub 2016 Aug 09.

Granulation tissue formation requires a robust angiogenic response. As granulation tissue develops, collagen fibers are deposited and compacted. Forces generated in the wake of this process drive wound contraction to reduce the wound area. In diabetics, both angiogenesis and...

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Lim NS, Sham A, Chee SM, et al. Combination of ciclopirox olamine and sphingosine-1-phosphate as granulation enhancer in diabetic wounds. Wound Repair Regen. 2016;24(5):795-809doi: 10.1111/wrr.12463.
Lim, N. S., Sham, A., Chee, S. M., Chan, C., & Raghunath, M. (2016). Combination of ciclopirox olamine and sphingosine-1-phosphate as granulation enhancer in diabetic wounds. Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society, 24(5), 795-809. https://doi.org/10.1111/wrr.12463
Lim, Natalie Sheng Jie, et al. "Combination of ciclopirox olamine and sphingosine-1-phosphate as granulation enhancer in diabetic wounds." Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society vol. 24,5 (2016): 795-809. doi: https://doi.org/10.1111/wrr.12463
Lim NS, Sham A, Chee SM, Chan C, Raghunath M. Combination of ciclopirox olamine and sphingosine-1-phosphate as granulation enhancer in diabetic wounds. Wound Repair Regen. 2016 Sep;24(5):795-809. doi: 10.1111/wrr.12463. Epub 2016 Aug 09. PMID: 27402256.
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Interleukin-34 in rheumatoid arthritis: potential role in clinical therapy.

International journal of clinical and experimental medicine

Zhang F, Ding R, Li P, Ma C, Song D, Wang X, Ma T, Bi L.
PMID: 26221333
Int J Clin Exp Med. 2015 May 15;8(5):7809-15. eCollection 2015.

OBJECTIVE: To investigate, whether interleukin (IL)-34 can be used as marker for treatment effectiveness in rheumatoid arthritis (RA).METHODS: Serum samples were collected from 35 healthy participants and 83 patients with RA before as well as 4 weeks and 12...

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Zhang F, Ding R, Li P, et al. Interleukin-34 in rheumatoid arthritis: potential role in clinical therapy. Int J Clin Exp Med. 2015;8(5):7809-15
Zhang, F., Ding, R., Li, P., Ma, C., Song, D., Wang, X., Ma, T., & Bi, L. (2015). Interleukin-34 in rheumatoid arthritis: potential role in clinical therapy. International journal of clinical and experimental medicine, 8(5), 7809-15.
Zhang, Fangze, et al. "Interleukin-34 in rheumatoid arthritis: potential role in clinical therapy." International journal of clinical and experimental medicine vol. 8,5 (2015): 7809-15.
Zhang F, Ding R, Li P, Ma C, Song D, Wang X, Ma T, Bi L. Interleukin-34 in rheumatoid arthritis: potential role in clinical therapy. Int J Clin Exp Med. 2015 May 15;8(5):7809-15. eCollection 2015. PMID: 26221333; PMCID: PMC4509278.
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Cartilage oligomeric matrix protein in serum and synovial fluid of rheumatoid arthritis: potential use as a marker for joint cartilage damage.

Modern rheumatology

Momohara S, Yamanaka H, Holledge MM, Mizumura T, Ikari K, Okada N, Kamatani N, Tomatsu T.
PMID: 17143693
Mod Rheumatol. 2004;14(5):356-60. doi: 10.1007/s10165-004-0323-4.

This study examined the serum and synovial fluid concentrations of cartilage oligomeric matrix protein (COMP) in relation to the evolution of joint cartilage damage and the requirement for surgery in 125 patients with rheumatoid arthritis (RA). We compared the...

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Momohara S, Yamanaka H, Holledge MM, et al. Cartilage oligomeric matrix protein in serum and synovial fluid of rheumatoid arthritis: potential use as a marker for joint cartilage damage. Mod Rheumatol. 2004;14(5):356-60doi: 10.1007/s10165-004-0323-4.
Momohara, S., Yamanaka, H., Holledge, M. M., Mizumura, T., Ikari, K., Okada, N., Kamatani, N., & Tomatsu, T. (2004). Cartilage oligomeric matrix protein in serum and synovial fluid of rheumatoid arthritis: potential use as a marker for joint cartilage damage. Modern rheumatology, 14(5), 356-60. https://doi.org/10.1007/s10165-004-0323-4
Momohara, Shigeki, et al. "Cartilage oligomeric matrix protein in serum and synovial fluid of rheumatoid arthritis: potential use as a marker for joint cartilage damage." Modern rheumatology vol. 14,5 (2004): 356-60. doi: https://doi.org/10.1007/s10165-004-0323-4
Momohara S, Yamanaka H, Holledge MM, Mizumura T, Ikari K, Okada N, Kamatani N, Tomatsu T. Cartilage oligomeric matrix protein in serum and synovial fluid of rheumatoid arthritis: potential use as a marker for joint cartilage damage. Mod Rheumatol. 2004;14(5):356-60. doi: 10.1007/s10165-004-0323-4. PMID: 17143693.
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Cytogenetic analysis of the pathology of frozen shoulder.

International journal of shoulder surgery

Kabbabe B, Ramkumar S, Richardson M.
PMID: 21472067
Int J Shoulder Surg. 2010 Jul;4(3):75-8. doi: 10.4103/0973-6042.76966.

BACKGROUND: Frozen shoulder (FS) is a debilitating musculoskeletal condition with an uncertain etiology and pathogenic mechanism. The aim of this study was to investigate the hypothesis that an alteration in the level of cytokines may disrupt the normal inflammatory...

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Kabbabe B, Ramkumar S, Richardson M. Cytogenetic analysis of the pathology of frozen shoulder. Int J Shoulder Surg. 2010;4(3):75-8doi: 10.4103/0973-6042.76966.
Kabbabe, B., Ramkumar, S., & Richardson, M. (2010). Cytogenetic analysis of the pathology of frozen shoulder. International journal of shoulder surgery, 4(3), 75-8. https://doi.org/10.4103/0973-6042.76966
Kabbabe, Benjamin, et al. "Cytogenetic analysis of the pathology of frozen shoulder." International journal of shoulder surgery vol. 4,3 (2010): 75-8. doi: https://doi.org/10.4103/0973-6042.76966
Kabbabe B, Ramkumar S, Richardson M. Cytogenetic analysis of the pathology of frozen shoulder. Int J Shoulder Surg. 2010 Jul;4(3):75-8. doi: 10.4103/0973-6042.76966. PMID: 21472067; PMCID: PMC3063346.
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Expression of MMP-3 and TIMP-3 in gastric cancer tissue and its clinical significance.

Oncology letters

Liu HQ, Song S, Wang JH, Zhang SL.
PMID: 22848309
Oncol Lett. 2011 Nov;2(6):1319-1322. doi: 10.3892/ol.2011.399. Epub 2011 Aug 31.

The present study aimed to investigate the expression of matrix metalloproteinase-3 (MMP-3) and the tissue inhibitor of metalloproteinase-3 (TIMP-3) in gastric cancer tissue, as well as to analyze the correlation between their expression and the occurrence of gastric cancer....

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Liu HQ, Song S, Wang JH, et al. Expression of MMP-3 and TIMP-3 in gastric cancer tissue and its clinical significance. Oncol Lett. 2011;2(6):1319-1322doi: 10.3892/ol.2011.399.
Liu, H. Q., Song, S., Wang, J. H., & Zhang, S. L. (2011). Expression of MMP-3 and TIMP-3 in gastric cancer tissue and its clinical significance. Oncology letters, 2(6), 1319-1322. https://doi.org/10.3892/ol.2011.399
Liu, Hong-Qi, et al. "Expression of MMP-3 and TIMP-3 in gastric cancer tissue and its clinical significance." Oncology letters vol. 2,6 (2011): 1319-1322. doi: https://doi.org/10.3892/ol.2011.399
Liu HQ, Song S, Wang JH, Zhang SL. Expression of MMP-3 and TIMP-3 in gastric cancer tissue and its clinical significance. Oncol Lett. 2011 Nov;2(6):1319-1322. doi: 10.3892/ol.2011.399. Epub 2011 Aug 31. PMID: 22848309; PMCID: PMC3406489.
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Curcumin reduces prostaglandin E2, matrix metalloproteinase-3 and proteoglycan release in the secretome of interleukin 1β-treated articular cartilage.

F1000Research

Clutterbuck AL, Allaway D, Harris P, Mobasheri A.
PMID: 24555068
F1000Res. 2013 Jul 04;2:147. doi: 10.12688/f1000research.2-147.v2. eCollection 2013.

OBJECTIVE: Curcumin (diferuloylmethane) is a phytochemical with potent anti-inflammatory and anti-oxidant properties, and has therapeutic potential for the treatment of a range of inflammatory diseases, including osteoarthritis (OA). The aim of this study was to determine whether non-toxic concentrations...

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Clutterbuck AL, Allaway D, Harris P, et al. Curcumin reduces prostaglandin E2, matrix metalloproteinase-3 and proteoglycan release in the secretome of interleukin 1β-treated articular cartilage. F1000Res. 2013;2:147doi: 10.12688/f1000research.2-147.v2.
Clutterbuck, A. L., Allaway, D., Harris, P., & Mobasheri, A. (2013). Curcumin reduces prostaglandin E2, matrix metalloproteinase-3 and proteoglycan release in the secretome of interleukin 1β-treated articular cartilage. F1000Research, 2147. https://doi.org/10.12688/f1000research.2-147.v2
Clutterbuck, Abigail L, et al. "Curcumin reduces prostaglandin E2, matrix metalloproteinase-3 and proteoglycan release in the secretome of interleukin 1β-treated articular cartilage." F1000Research vol. 2 (2013): 147. doi: https://doi.org/10.12688/f1000research.2-147.v2
Clutterbuck AL, Allaway D, Harris P, Mobasheri A. Curcumin reduces prostaglandin E2, matrix metalloproteinase-3 and proteoglycan release in the secretome of interleukin 1β-treated articular cartilage. F1000Res. 2013 Jul 04;2:147. doi: 10.12688/f1000research.2-147.v2. eCollection 2013. PMID: 24555068; PMCID: PMC3901452.
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Predictor of the Simplified Disease Activity Index 50 (SDAI 50) at Month 3 of bDMARD Treatment in Patients with Long-Established Rheumatoid Arthritis.

The open rheumatology journal

Miwa Y, Saito M, Furuya H, Yanai R, Kasama T, Carmody M.
PMID: 29290847
Open Rheumatol J. 2017 Sep 30;11:106-112. doi: 10.2174/1874312901711010106. eCollection 2017.

OBJECTIVES: The Simplified Disease Activity Index (SDAI) 50 has good agreement with European League Against Rheumatism (EULAR) response measures for early Rheumatoid Arthritis (RA). There have been reports on early RA, but not on long-established RA. In this study,...

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Miwa Y, Saito M, Furuya H, et al. Predictor of the Simplified Disease Activity Index 50 (SDAI 50) at Month 3 of bDMARD Treatment in Patients with Long-Established Rheumatoid Arthritis. Open Rheumatol J. 2017;11:106-112doi: 10.2174/1874312901711010106.
Miwa, Y., Saito, M., Furuya, H., Yanai, R., Kasama, T., & Carmody, M. (2017). Predictor of the Simplified Disease Activity Index 50 (SDAI 50) at Month 3 of bDMARD Treatment in Patients with Long-Established Rheumatoid Arthritis. The open rheumatology journal, 11106-112. https://doi.org/10.2174/1874312901711010106
Miwa, Yusuke, et al. "Predictor of the Simplified Disease Activity Index 50 (SDAI 50) at Month 3 of bDMARD Treatment in Patients with Long-Established Rheumatoid Arthritis." The open rheumatology journal vol. 11 (2017): 106-112. doi: https://doi.org/10.2174/1874312901711010106
Miwa Y, Saito M, Furuya H, Yanai R, Kasama T, Carmody M. Predictor of the Simplified Disease Activity Index 50 (SDAI 50) at Month 3 of bDMARD Treatment in Patients with Long-Established Rheumatoid Arthritis. Open Rheumatol J. 2017 Sep 30;11:106-112. doi: 10.2174/1874312901711010106. eCollection 2017. PMID: 29290847; PMCID: PMC5737026.
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Degenerate intervertebral disc-like pH induces a catabolic mechanoresponse in human nucleus pulposus cells.

JOR spine

Hodson NW, Patel S, Richardson SM, Hoyland JA, Gilbert HTJ.
PMID: 31463436
JOR Spine. 2018 Mar 11;1(1):e1004. doi: 10.1002/jsp2.1004. eCollection 2018 Mar.

Mechanical stimulation is known to influence intervertebral disc (IVD) cell behavior and function, but the effect on disc cells is routinely considered in isolation from other microenvironmental factors. Acidic pH has been shown to be a prominent and detrimental...

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Hodson NW, Patel S, Richardson SM, et al. Degenerate intervertebral disc-like pH induces a catabolic mechanoresponse in human nucleus pulposus cells. JOR Spine. 2018;1(1):e1004doi: 10.1002/jsp2.1004.
Hodson, N. W., Patel, S., Richardson, S. M., Hoyland, J. A., & Gilbert, H. T. J. (2018). Degenerate intervertebral disc-like pH induces a catabolic mechanoresponse in human nucleus pulposus cells. JOR spine, 1(1), e1004. https://doi.org/10.1002/jsp2.1004
Hodson, Nathan W, et al. "Degenerate intervertebral disc-like pH induces a catabolic mechanoresponse in human nucleus pulposus cells." JOR spine vol. 1,1 (2018): e1004. doi: https://doi.org/10.1002/jsp2.1004
Hodson NW, Patel S, Richardson SM, Hoyland JA, Gilbert HTJ. Degenerate intervertebral disc-like pH induces a catabolic mechanoresponse in human nucleus pulposus cells. JOR Spine. 2018 Mar 11;1(1):e1004. doi: 10.1002/jsp2.1004. eCollection 2018 Mar. PMID: 31463436; PMCID: PMC6711490.
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Matrix metalloproteinases 3 polymorphism increases the risk of developing advanced endometriosis and infertility: A case-control study.

European journal of obstetrics & gynecology and reproductive biology: X

Cardoso JV, Machado DE, da Silva MC, Berardo PT, Ferrari R, Abrão MS, Perini JA.
PMID: 31404425
Eur J Obstet Gynecol Reprod Biol X. 2019 May 06;3:100041. doi: 10.1016/j.eurox.2019.100041. eCollection 2019 Jul.

OBJECTIVE: Endometriosis has a complex and multifactorial pathology, and it is considered one of the main causes of infertility nowadays. The angiogenic process, which involves remodeling of extracellular matrix, is crucial for the development of this disease, mainly by...

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Cardoso JV, Machado DE, da Silva MC, et al. Matrix metalloproteinases 3 polymorphism increases the risk of developing advanced endometriosis and infertility: A case-control study. Eur J Obstet Gynecol Reprod Biol X. 2019;3:100041doi: 10.1016/j.eurox.2019.100041.
Cardoso, J. V., Machado, D. E., da Silva, M. C., Berardo, P. T., Ferrari, R., Abrão, M. S., & Perini, J. A. (2019). Matrix metalloproteinases 3 polymorphism increases the risk of developing advanced endometriosis and infertility: A case-control study. European journal of obstetrics & gynecology and reproductive biology: X, 3100041. https://doi.org/10.1016/j.eurox.2019.100041
Cardoso, Jéssica V, et al. "Matrix metalloproteinases 3 polymorphism increases the risk of developing advanced endometriosis and infertility: A case-control study." European journal of obstetrics & gynecology and reproductive biology: X vol. 3 (2019): 100041. doi: https://doi.org/10.1016/j.eurox.2019.100041
Cardoso JV, Machado DE, da Silva MC, Berardo PT, Ferrari R, Abrão MS, Perini JA. Matrix metalloproteinases 3 polymorphism increases the risk of developing advanced endometriosis and infertility: A case-control study. Eur J Obstet Gynecol Reprod Biol X. 2019 May 06;3:100041. doi: 10.1016/j.eurox.2019.100041. eCollection 2019 Jul. PMID: 31404425; PMCID: PMC6687389.
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Role of oxidative stress in Parkinson's disease.

Experimental neurobiology

Hwang O.
PMID: 23585717
Exp Neurobiol. 2013 Mar;22(1):11-7. doi: 10.5607/en.2013.22.1.11. Epub 2013 Mar 31.

Parkinson's disease (PD) is a progressive neurodegenerative movement disorder associated with a selective loss of the dopamine(DA)rgic neurons in the substantia nigra pars compacta and the degeneration of projecting nerve fibers in the striatum. Because there is currently no...

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Hwang O. Role of oxidative stress in Parkinson's disease. Exp Neurobiol. 2013;22(1):11-7doi: 10.5607/en.2013.22.1.11.
Hwang, O. (2013). Role of oxidative stress in Parkinson's disease. Experimental neurobiology, 22(1), 11-7. https://doi.org/10.5607/en.2013.22.1.11
Hwang, Onyou. "Role of oxidative stress in Parkinson's disease." Experimental neurobiology vol. 22,1 (2013): 11-7. doi: https://doi.org/10.5607/en.2013.22.1.11
Hwang O. Role of oxidative stress in Parkinson's disease. Exp Neurobiol. 2013 Mar;22(1):11-7. doi: 10.5607/en.2013.22.1.11. Epub 2013 Mar 31. PMID: 23585717; PMCID: PMC3620453.
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Showing 1 to 12 of 202 entries