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Tissue Biomarkers in Hepatocellular Tumors: Which, When, and How.

Frontiers in medicine

Di Tommaso L, Roncalli M.
PMID: 28280721
Front Med (Lausanne). 2017 Feb 23;4:10. doi: 10.3389/fmed.2017.00010. eCollection 2017.

Few tissue markers are currently available to pathologists in the study of hepatocellular tumors. These markers should be used carefully taking into consideration not only morphology but also, and sometimes even more important, the clinical setting where the lesion...

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Di Tommaso L, Roncalli M. Tissue Biomarkers in Hepatocellular Tumors: Which, When, and How. Front Med (Lausanne). 2017;4:10doi: 10.3389/fmed.2017.00010.
Di Tommaso, L., & Roncalli, M. (2017). Tissue Biomarkers in Hepatocellular Tumors: Which, When, and How. Frontiers in medicine, 410. https://doi.org/10.3389/fmed.2017.00010
Di Tommaso, Luca, and Roncalli, Massimo. "Tissue Biomarkers in Hepatocellular Tumors: Which, When, and How." Frontiers in medicine vol. 4 (2017): 10. doi: https://doi.org/10.3389/fmed.2017.00010
Di Tommaso L, Roncalli M. Tissue Biomarkers in Hepatocellular Tumors: Which, When, and How. Front Med (Lausanne). 2017 Feb 23;4:10. doi: 10.3389/fmed.2017.00010. eCollection 2017. PMID: 28280721; PMCID: PMC5322593.
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Eosinophil recruitment and activation: the role of lipid mediators.

Frontiers in pharmacology

Luna-Gomes T, Bozza PT, Bandeira-Melo C.
PMID: 23525348
Front Pharmacol. 2013 Mar 22;4:27. doi: 10.3389/fphar.2013.00027. eCollection 2013.

Eosinophils are effector cells that migrate toward several mediators released at inflammatory sites to perform their multiple functions. The mechanisms driving eosinophil selective accumulation in sites of allergic inflammation are well-established and involve several steps controlled by adhesion molecules,...

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Luna-Gomes T, Bozza PT, Bandeira-Melo C. Eosinophil recruitment and activation: the role of lipid mediators. Front Pharmacol. 2013;4:27doi: 10.3389/fphar.2013.00027.
Luna-Gomes, T., Bozza, P. T., & Bandeira-Melo, C. (2013). Eosinophil recruitment and activation: the role of lipid mediators. Frontiers in pharmacology, 427. https://doi.org/10.3389/fphar.2013.00027
Luna-Gomes, Tatiana, et al. "Eosinophil recruitment and activation: the role of lipid mediators." Frontiers in pharmacology vol. 4 (2013): 27. doi: https://doi.org/10.3389/fphar.2013.00027
Luna-Gomes T, Bozza PT, Bandeira-Melo C. Eosinophil recruitment and activation: the role of lipid mediators. Front Pharmacol. 2013 Mar 22;4:27. doi: 10.3389/fphar.2013.00027. eCollection 2013. PMID: 23525348; PMCID: PMC3605515.
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Imperatorin Suppresses Degranulation and Eicosanoid Generation in Activated Bone Marrow-Derived Mast Cells.

Biomolecules & therapeutics

Jeong KT, Lee E, Park NY, Kim SG, Park HH, Lee J, Lee YJ, Lee E.
PMID: 26336581
Biomol Ther (Seoul). 2015 Sep;23(5):421-7. doi: 10.4062/biomolther.2015.023. Epub 2015 Sep 01.

Imperatorin has been known to exert many biological functions including anti-inflammatory activity. In this study, we investigated the inhibitory effects of imperatorin on the production of inflammatory mediators in mouse bone marrow-derived mast cells (BMMC). Imperatorin inhibited degranulation and...

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Jeong KT, Lee E, Park NY, et al. Imperatorin Suppresses Degranulation and Eicosanoid Generation in Activated Bone Marrow-Derived Mast Cells. Biomol Ther (Seoul). 2015;23(5):421-7doi: 10.4062/biomolther.2015.023.
Jeong, K. T., Lee, E., Park, N. Y., Kim, S. G., Park, H. H., Lee, J., Lee, Y. J., & Lee, E. (2015). Imperatorin Suppresses Degranulation and Eicosanoid Generation in Activated Bone Marrow-Derived Mast Cells. Biomolecules & therapeutics, 23(5), 421-7. https://doi.org/10.4062/biomolther.2015.023
Jeong, Kyu-Tae, et al. "Imperatorin Suppresses Degranulation and Eicosanoid Generation in Activated Bone Marrow-Derived Mast Cells." Biomolecules & therapeutics vol. 23,5 (2015): 421-7. doi: https://doi.org/10.4062/biomolther.2015.023
Jeong KT, Lee E, Park NY, Kim SG, Park HH, Lee J, Lee YJ, Lee E. Imperatorin Suppresses Degranulation and Eicosanoid Generation in Activated Bone Marrow-Derived Mast Cells. Biomol Ther (Seoul). 2015 Sep;23(5):421-7. doi: 10.4062/biomolther.2015.023. Epub 2015 Sep 01. PMID: 26336581; PMCID: PMC4556201.
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Detection of allergic reactions during oral food challenge using noninvasive urinary prostaglandin D2 metabolites.

Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology

Inuzuka Y, Yamamoto-Hanada K, Nakamura T, Shimosawa T, Murata T, Ohya Y.
PMID: 34460978
Clin Exp Allergy. 2022 Jan;52(1):176-179. doi: 10.1111/cea.14006. Epub 2021 Sep 05.

No abstract available.

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Inuzuka Y, Yamamoto-Hanada K, Nakamura T, et al. Detection of allergic reactions during oral food challenge using noninvasive urinary prostaglandin D2 metabolites. Clin Exp Allergy. 2021;52(1):176-179doi: 10.1111/cea.14006.
Inuzuka, Y., Yamamoto-Hanada, K., Nakamura, T., Shimosawa, T., Murata, T., & Ohya, Y. (2022). Detection of allergic reactions during oral food challenge using noninvasive urinary prostaglandin D2 metabolites. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology, 52(1), 176-179. https://doi.org/10.1111/cea.14006
Inuzuka, Yusuke, et al. "Detection of allergic reactions during oral food challenge using noninvasive urinary prostaglandin D2 metabolites." Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology vol. 52,1 (2022): 176-179. doi: https://doi.org/10.1111/cea.14006
Inuzuka Y, Yamamoto-Hanada K, Nakamura T, Shimosawa T, Murata T, Ohya Y. Detection of allergic reactions during oral food challenge using noninvasive urinary prostaglandin D2 metabolites. Clin Exp Allergy. 2022 Jan;52(1):176-179. doi: 10.1111/cea.14006. Epub 2021 Sep 05. PMID: 34460978.
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Protective Effect of Low-Dose Alcohol Consumption against Post-Ischemic Neuronal Apoptosis: Role of L-PGDS.

International journal of molecular sciences

Li C, Li J, Loreno EG, Miriyala S, Panchatcharam M, Sun H.
PMID: 35008575
Int J Mol Sci. 2021 Dec 23;23(1). doi: 10.3390/ijms23010133.

Ischemic stroke is one of the leading causes of permanent disability and death in adults worldwide. Apoptosis is a major element contributing to post-ischemic neuronal death. We previously found that low-dose alcohol consumption (LAC) protects against neuronal apoptosis in...

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Li C, Li J, Loreno EG, et al. Protective Effect of Low-Dose Alcohol Consumption against Post-Ischemic Neuronal Apoptosis: Role of L-PGDS. Int J Mol Sci. 2021;23(1)doi: 10.3390/ijms23010133.
Li, C., Li, J., Loreno, E. G., Miriyala, S., Panchatcharam, M., & Sun, H. (2021). Protective Effect of Low-Dose Alcohol Consumption against Post-Ischemic Neuronal Apoptosis: Role of L-PGDS. International journal of molecular sciences, 23(1), . https://doi.org/10.3390/ijms23010133
Li, Chun, et al. "Protective Effect of Low-Dose Alcohol Consumption against Post-Ischemic Neuronal Apoptosis: Role of L-PGDS." International journal of molecular sciences vol. 23,1 (2021). doi: https://doi.org/10.3390/ijms23010133
Li C, Li J, Loreno EG, Miriyala S, Panchatcharam M, Sun H. Protective Effect of Low-Dose Alcohol Consumption against Post-Ischemic Neuronal Apoptosis: Role of L-PGDS. Int J Mol Sci. 2021 Dec 23;23(1). doi: 10.3390/ijms23010133. PMID: 35008575.
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Protective Effect of Low-Dose Alcohol Consumption against Post-Ischemic Neuronal Apoptosis: Role of L-PGDS.

International journal of molecular sciences

Li C, Li J, Loreno EG, Miriyala S, Panchatcharam M, Sun H.
PMID: 35008575
Int J Mol Sci. 2021 Dec 23;23(1). doi: 10.3390/ijms23010133.

Ischemic stroke is one of the leading causes of permanent disability and death in adults worldwide. Apoptosis is a major element contributing to post-ischemic neuronal death. We previously found that low-dose alcohol consumption (LAC) protects against neuronal apoptosis in...

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Li C, Li J, Loreno EG, et al. Protective Effect of Low-Dose Alcohol Consumption against Post-Ischemic Neuronal Apoptosis: Role of L-PGDS. Int J Mol Sci. 2021;23(1)doi: 10.3390/ijms23010133.
Li, C., Li, J., Loreno, E. G., Miriyala, S., Panchatcharam, M., & Sun, H. (2021). Protective Effect of Low-Dose Alcohol Consumption against Post-Ischemic Neuronal Apoptosis: Role of L-PGDS. International journal of molecular sciences, 23(1), . https://doi.org/10.3390/ijms23010133
Li, Chun, et al. "Protective Effect of Low-Dose Alcohol Consumption against Post-Ischemic Neuronal Apoptosis: Role of L-PGDS." International journal of molecular sciences vol. 23,1 (2021). doi: https://doi.org/10.3390/ijms23010133
Li C, Li J, Loreno EG, Miriyala S, Panchatcharam M, Sun H. Protective Effect of Low-Dose Alcohol Consumption against Post-Ischemic Neuronal Apoptosis: Role of L-PGDS. Int J Mol Sci. 2021 Dec 23;23(1). doi: 10.3390/ijms23010133. PMID: 35008575.
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Correction to "Absorption, Distribution, Metabolism, and Excretion of the Oral Prostaglandin D2 Receptor 2 Antagonist Fevipiprant (QAW039) in Healthy Volunteers and In Vitro".

Drug metabolism and disposition: the biological fate of chemicals

[No authors listed]
PMID: 33593806
Drug Metab Dispos. 2021 Mar;49(3):287-288. doi: 10.1124/dmd.117.075358err.

No abstract available.

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Correction to "Absorption, Distribution, Metabolism, and Excretion of the Oral Prostaglandin D2 Receptor 2 Antagonist Fevipiprant (QAW039) in Healthy Volunteers and In Vitro". Drug Metab Dispos. 2021;49(3):287-288doi: 10.1124/dmd.117.075358err.
(2021). Correction to "Absorption, Distribution, Metabolism, and Excretion of the Oral Prostaglandin D2 Receptor 2 Antagonist Fevipiprant (QAW039) in Healthy Volunteers and In Vitro". Drug metabolism and disposition: the biological fate of chemicals, 49(3), 287-288. https://doi.org/10.1124/dmd.117.075358err
"Correction to "Absorption, Distribution, Metabolism, and Excretion of the Oral Prostaglandin D2 Receptor 2 Antagonist Fevipiprant (QAW039) in Healthy Volunteers and In Vitro"." Drug metabolism and disposition: the biological fate of chemicals vol. 49,3 (2021): 287-288. doi: https://doi.org/10.1124/dmd.117.075358err
Correction to "Absorption, Distribution, Metabolism, and Excretion of the Oral Prostaglandin D2 Receptor 2 Antagonist Fevipiprant (QAW039) in Healthy Volunteers and In Vitro". Drug Metab Dispos. 2021 Mar;49(3):287-288. doi: 10.1124/dmd.117.075358err. PMID: 33593806.
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Catalysis-Enabled Concise and Stereoselective Total Synthesis of the Tricyclic Prostaglandin D2 Metabolite Methyl Ester.

Angewandte Chemie (International ed. in English)

Dai M, Sims HS, de Andrade Horn P, Isshiki R, Lim M, Xu Y, Grubbs RH.
PMID: 34870881
Angew Chem Int Ed Engl. 2021 Dec 06; doi: 10.1002/anie.202115633. Epub 2021 Dec 06.

A concise and stereoselective total synthesis of the clinically relevant tricyclic prostaglandin D 2 metabolite (tricyclic-PGDM) methyl ester in racemic form was accomplished in 8 steps from a readily available known cyclopentene-diol derivative. The synthesis features a nickel-catalyzed Ueno-Stork-type...

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Dai M, Sims HS, de Andrade Horn P, et al. Catalysis-Enabled Concise and Stereoselective Total Synthesis of the Tricyclic Prostaglandin D2 Metabolite Methyl Ester. Angew Chem Int Ed Engl. 2021;doi: 10.1002/anie.202115633.
Dai, M., Sims, H. S., de Andrade Horn, P., Isshiki, R., Lim, M., Xu, Y., & Grubbs, R. H. (2021). Catalysis-Enabled Concise and Stereoselective Total Synthesis of the Tricyclic Prostaglandin D2 Metabolite Methyl Ester. Angewandte Chemie (International ed. in English), . https://doi.org/10.1002/anie.202115633
Dai, Mingji, et al. "Catalysis-Enabled Concise and Stereoselective Total Synthesis of the Tricyclic Prostaglandin D2 Metabolite Methyl Ester." Angewandte Chemie (International ed. in English) vol. (2021). doi: https://doi.org/10.1002/anie.202115633
Dai M, Sims HS, de Andrade Horn P, Isshiki R, Lim M, Xu Y, Grubbs RH. Catalysis-Enabled Concise and Stereoselective Total Synthesis of the Tricyclic Prostaglandin D2 Metabolite Methyl Ester. Angew Chem Int Ed Engl. 2021 Dec 06; doi: 10.1002/anie.202115633. Epub 2021 Dec 06. PMID: 34870881.
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Label-Free, Novel Electrofluidic Capacitor Biosensor for Prostaglandin E2 Detection toward Early and Rapid Urinary Tract Infection Diagnosis.

ACS sensors

Ganguly A, Ebrahimzadeh T, Zimmern P, De Nisco NJ, Prasad S.
PMID: 34928577
ACS Sens. 2021 Dec 20; doi: 10.1021/acssensors.1c01951. Epub 2021 Dec 20.

Urine Prostaglandin E2 (PGE2) has been identified as an attractive diagnostic and prognostic biomarker for urinary tract infection (UTI). This work demonstrates the use of PGE2 as a biomarker for rapid and label-free testing for UTI. In this work,...

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Ganguly A, Ebrahimzadeh T, Zimmern P, et al. Label-Free, Novel Electrofluidic Capacitor Biosensor for Prostaglandin E2 Detection toward Early and Rapid Urinary Tract Infection Diagnosis. ACS Sens. 2021;doi: 10.1021/acssensors.1c01951.
Ganguly, A., Ebrahimzadeh, T., Zimmern, P., De Nisco, N. J., & Prasad, S. (2021). Label-Free, Novel Electrofluidic Capacitor Biosensor for Prostaglandin E2 Detection toward Early and Rapid Urinary Tract Infection Diagnosis. ACS sensors, . https://doi.org/10.1021/acssensors.1c01951
Ganguly, Antra, et al. "Label-Free, Novel Electrofluidic Capacitor Biosensor for Prostaglandin E2 Detection toward Early and Rapid Urinary Tract Infection Diagnosis." ACS sensors vol. (2021). doi: https://doi.org/10.1021/acssensors.1c01951
Ganguly A, Ebrahimzadeh T, Zimmern P, De Nisco NJ, Prasad S. Label-Free, Novel Electrofluidic Capacitor Biosensor for Prostaglandin E2 Detection toward Early and Rapid Urinary Tract Infection Diagnosis. ACS Sens. 2021 Dec 20; doi: 10.1021/acssensors.1c01951. Epub 2021 Dec 20. PMID: 34928577.
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DP1 prostanoid receptor activation increases the severity of an acute lower respiratory viral infection in mice via TNF-α-induced immunopathology.

Mucosal immunology

Ullah MA, Rittchen S, Li J, Hasnain SZ, Phipps S.
PMID: 33879829
Mucosal Immunol. 2021 Jul;14(4):963-972. doi: 10.1038/s41385-021-00405-7. Epub 2021 Apr 20.

Respiratory syncytial virus (RSV) bronchiolitis is a leading cause of infant hospitalization and mortality. We previously identified that prostaglandin D2 (PGD2), released following RSV infection of primary human airway epithelial cells or pneumonia virus of mice (PVM) infection of...

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Ullah MA, Rittchen S, Li J, et al. DP1 prostanoid receptor activation increases the severity of an acute lower respiratory viral infection in mice via TNF-α-induced immunopathology. Mucosal Immunol. 2021;14(4):963-972doi: 10.1038/s41385-021-00405-7.
Ullah, M. A., Rittchen, S., Li, J., Hasnain, S. Z., & Phipps, S. (2021). DP1 prostanoid receptor activation increases the severity of an acute lower respiratory viral infection in mice via TNF-α-induced immunopathology. Mucosal immunology, 14(4), 963-972. https://doi.org/10.1038/s41385-021-00405-7
Ullah, Md Ashik, et al. "DP1 prostanoid receptor activation increases the severity of an acute lower respiratory viral infection in mice via TNF-α-induced immunopathology." Mucosal immunology vol. 14,4 (2021): 963-972. doi: https://doi.org/10.1038/s41385-021-00405-7
Ullah MA, Rittchen S, Li J, Hasnain SZ, Phipps S. DP1 prostanoid receptor activation increases the severity of an acute lower respiratory viral infection in mice via TNF-α-induced immunopathology. Mucosal Immunol. 2021 Jul;14(4):963-972. doi: 10.1038/s41385-021-00405-7. Epub 2021 Apr 20. PMID: 33879829; PMCID: PMC8057290.
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Plant Sterol-Poor Diet Is Associated with Pro-Inflammatory Lipid Mediators in the Murine Brain.

International journal of molecular sciences

Reinicke M, Leyh J, Zimmermann S, Chey S, Brkovic IB, Wassermann C, Landmann J, Lütjohann D, Isermann B, Bechmann I, Ceglarek U.
PMID: 34948003
Int J Mol Sci. 2021 Dec 08;22(24). doi: 10.3390/ijms222413207.

Plant sterols (PSs) cannot be synthesized in mammals and are exclusively diet-derived. PSs cross the blood-brain barrier and may have anti-neuroinflammatory effects. Obesity is linked to lower intestinal uptake and blood levels of PSs, but its effects in terms...

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Reinicke M, Leyh J, Zimmermann S, et al. Plant Sterol-Poor Diet Is Associated with Pro-Inflammatory Lipid Mediators in the Murine Brain. Int J Mol Sci. 2021;22(24)doi: 10.3390/ijms222413207.
Reinicke, M., Leyh, J., Zimmermann, S., Chey, S., Brkovic, I. B., Wassermann, C., Landmann, J., Lütjohann, D., Isermann, B., Bechmann, I., & Ceglarek, U. (2021). Plant Sterol-Poor Diet Is Associated with Pro-Inflammatory Lipid Mediators in the Murine Brain. International journal of molecular sciences, 22(24), . https://doi.org/10.3390/ijms222413207
Reinicke, Madlen, et al. "Plant Sterol-Poor Diet Is Associated with Pro-Inflammatory Lipid Mediators in the Murine Brain." International journal of molecular sciences vol. 22,24 (2021). doi: https://doi.org/10.3390/ijms222413207
Reinicke M, Leyh J, Zimmermann S, Chey S, Brkovic IB, Wassermann C, Landmann J, Lütjohann D, Isermann B, Bechmann I, Ceglarek U. Plant Sterol-Poor Diet Is Associated with Pro-Inflammatory Lipid Mediators in the Murine Brain. Int J Mol Sci. 2021 Dec 08;22(24). doi: 10.3390/ijms222413207. PMID: 34948003.
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Molecular basis for lipid recognition by the prostaglandin D.

Proceedings of the National Academy of Sciences of the United States of America

Liu H, Deepak RNVK, Shiriaeva A, Gati C, Batyuk A, Hu H, Weierstall U, Liu W, Wang L, Cherezov V, Fan H, Zhang C.
PMID: 34341104
Proc Natl Acad Sci U S A. 2021 Aug 10;118(32). doi: 10.1073/pnas.2102813118.

Prostaglandin D

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Liu H, Deepak RNVK, Shiriaeva A, et al. Molecular basis for lipid recognition by the prostaglandin D. Proc Natl Acad Sci U S A. 2021;118(32)doi: 10.1073/pnas.2102813118.
Liu, H., Deepak, R. N. V. K., Shiriaeva, A., Gati, C., Batyuk, A., Hu, H., Weierstall, U., Liu, W., Wang, L., Cherezov, V., Fan, H., & Zhang, C. (2021). Molecular basis for lipid recognition by the prostaglandin D. Proceedings of the National Academy of Sciences of the United States of America, 118(32), . https://doi.org/10.1073/pnas.2102813118
Liu, Heng, et al. "Molecular basis for lipid recognition by the prostaglandin D." Proceedings of the National Academy of Sciences of the United States of America vol. 118,32 (2021). doi: https://doi.org/10.1073/pnas.2102813118
Liu H, Deepak RNVK, Shiriaeva A, Gati C, Batyuk A, Hu H, Weierstall U, Liu W, Wang L, Cherezov V, Fan H, Zhang C. Molecular basis for lipid recognition by the prostaglandin D. Proc Natl Acad Sci U S A. 2021 Aug 10;118(32). doi: 10.1073/pnas.2102813118. PMID: 34341104; PMCID: PMC8364189.
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Showing 1 to 12 of 90 entries