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  1. Article ; Online: Belvarafenib penetrates the BBB and shows potent antitumor activity in a murine melanoma brain metastasis model.

    Kim, Yu-Yon / Park, Hyunjin / Song, Taehun / Choi, Kyungjin / Dolton, Michael / Mao, Jialin / Kim, Jisook / Ahn, Young Gil / Suh, Kwee Hyun / Kim, Young Hoon

    Clinical & experimental metastasis

    2023  Volume 40, Issue 2, Page(s) 137–148

    Abstract: Brain metastasis is a common complication in melanoma patients with BRAF and NRAS mutations and has a poor prognosis. Although BRAF inhibitors are clinically approved, their poor brain penetration limits their efficacy in brain metastasis. Thus, melanoma ...

    Abstract Brain metastasis is a common complication in melanoma patients with BRAF and NRAS mutations and has a poor prognosis. Although BRAF inhibitors are clinically approved, their poor brain penetration limits their efficacy in brain metastasis. Thus, melanoma brain metastasis still requires better treatment. Belvarafenib, a pan-RAF inhibitor, has reported antitumor activity in melanoma with RAF and RAS mutations in animal models and patients. However, brain permeability and antitumor efficacy on brain metastasis have not been determined. This study confirmed the brain penetration of belvarafenib, the antitumor activity on BRAF and NRAS mutant melanoma, and the efficacy on melanoma within the brain. Belvarafenib strongly suppressed melanoma in BRAF V600E mutant A375SM tumor-bearing mice. It also significantly inhibited tumor growth in NRAS mutant SK-MEL-30 and K1735 tumor-bearing mice and synergized to enhance the antitumor activity combined with cobimetinib or atezolizumab. Belvarafenib was penetrated at considerable levels into the brains of mice and rats following oral administration. The exposure of belvarafenib in the brain was similar to or higher than that in plasma, and this high brain penetration differed significantly from that of other BRAF inhibitors with low brain penetration. Most importantly, belvarafenib strongly reduced tumor burden and markedly improved survival benefits in mice intracranially implanted with A375SM melanoma. These results demonstrated that belvarafenib, which has favorable BBB permeability, and potent antitumor activity on the tumors with BRAF/NRAS mutations, may be a promising therapeutic option for patients with BRAF/NRAS mutant melanoma brain metastasis.
    MeSH term(s) Mice ; Rats ; Animals ; Proto-Oncogene Proteins B-raf/genetics ; Melanoma/drug therapy ; Melanoma/genetics ; Melanoma/pathology ; Protein Kinase Inhibitors/therapeutic use ; Brain Neoplasms/drug therapy ; Mutation ; Cell Line, Tumor ; Skin Neoplasms/pathology
    Chemical Substances Proto-Oncogene Proteins B-raf (EC 2.7.11.1) ; Protein Kinase Inhibitors
    Language English
    Publishing date 2023-02-10
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 604952-7
    ISSN 1573-7276 ; 0262-0898
    ISSN (online) 1573-7276
    ISSN 0262-0898
    DOI 10.1007/s10585-023-10198-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Design and synthesis of 4th generation EGFR inhibitors against human triple (Del19/T790M/C797S) mutation.

    Jeon, Jiyoung / Jang, Sun Young / Kwak, Eun Joo / Lee, Sun Hoe / Byun, Joo-Yun / Kim, Yu-Yon / Ahn, Young Gil / Singh, Pargat / Moon, Kyeongwon / Kim, In Su

    European journal of medicinal chemistry

    2023  Volume 261, Page(s) 115840

    Abstract: Epidermal growth factor receptor (EGFR)-targeted therapy is used to treat EGFR mutation-induced non-small cell lung cancer (NSCLC). However, its efficacy does not last beyond a certain period due to the development of primary and secondary resistance. ... ...

    Abstract Epidermal growth factor receptor (EGFR)-targeted therapy is used to treat EGFR mutation-induced non-small cell lung cancer (NSCLC). However, its efficacy does not last beyond a certain period due to the development of primary and secondary resistance. First and second-generation inhibitors (e.g., gefitinib, erlotinib, and afatinib) induce EGFR T790M mutations, while third-generation inhibitors (e.g., osimertinib) induce C797S as a major target resistance mutation. Therefore, the C797S mutation is being actively researched. In this study, we investigated the structure-activity relationship of several synthesized compounds as fourth-generation inhibitors against the C797S mutation. We identified a compound 13k that displayed nanomolar potency and high selectivity. Moreover, we used a triple mutant xenograft mouse model to evaluate the in vivo efficacy of 13k in inhibiting EGFR C797S, which demonstrated exceptional profiles and satisfactory EGFR C797S inhibition efficacy. Based on its excellent in vitro and in vivo profiles, compound 13k can be considered a promising candidate for treating EGFR C797S mutations.
    MeSH term(s) Humans ; Animals ; Mice ; Carcinoma, Non-Small-Cell Lung/metabolism ; Mutation ; Lung Neoplasms/metabolism ; ErbB Receptors ; Protein Kinase Inhibitors/pharmacology ; Drug Resistance, Neoplasm ; Aniline Compounds/pharmacology
    Chemical Substances ErbB Receptors (EC 2.7.10.1) ; Protein Kinase Inhibitors ; Aniline Compounds ; EGFR protein, human (EC 2.7.10.1)
    Language English
    Publishing date 2023-09-27
    Publishing country France
    Document type Journal Article
    ZDB-ID 188597-2
    ISSN 1768-3254 ; 0009-4374 ; 0223-5234
    ISSN (online) 1768-3254
    ISSN 0009-4374 ; 0223-5234
    DOI 10.1016/j.ejmech.2023.115840
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  3. Article ; Online: Synergistic Effects of BTK Inhibitor HM71224 and Methotrexate in a Collagen-induced Arthritis Rat Model.

    Choi, Kyung Jin / Kim, Yu-Yon / Jang, Sun Young / Ahn, Young Gil / Suh, Kwee Hyun / Kim, Young Hoon / Kim, Hyung Sik

    In vivo (Athens, Greece)

    2021  Volume 35, Issue 6, Page(s) 3245–3251

    Abstract: Background/aim: Using a rat model of collagen-induced arthritis (CIA), we evaluated the therapeutic effects of HM71224 (BTKi), as well as the drug-drug interactions in combined therapy with methotrexate (MTX) based on both drugs' pharmacological role in ...

    Abstract Background/aim: Using a rat model of collagen-induced arthritis (CIA), we evaluated the therapeutic effects of HM71224 (BTKi), as well as the drug-drug interactions in combined therapy with methotrexate (MTX) based on both drugs' pharmacological role in immune regulation and antiinflammation.
    Materials and methods: Arthritis in rats was induced using type II collagen and incomplete Freund's adjuvant. The therapeutic effects of HM71224 (alone or in combination with MTX) were evaluated by arthritis score, paw volume, body weight, and histopathological examination (H&E and Safranin-O staining). The drug-drug interactions between HM71224 and MTX were investigated by measuring plasma, liver enzyme and creatinine levels and blood cell counts.
    Results: HM71224 reduced the clinical signs of arthritis, paw volume, and body weight loss in CIA rats. ED
    Conclusion: The combination of HM71224 and MTX improved the therapeutic effect with no drug-drug interactions in RA.
    MeSH term(s) Animals ; Anti-Inflammatory Agents/therapeutic use ; Arthritis, Experimental/drug therapy ; Drug Therapy, Combination ; Methotrexate/pharmacology ; Methotrexate/therapeutic use ; Protein Kinase Inhibitors/therapeutic use ; Rats
    Chemical Substances Anti-Inflammatory Agents ; Protein Kinase Inhibitors ; Methotrexate (YL5FZ2Y5U1)
    Language English
    Publishing date 2021-11-12
    Publishing country Greece
    Document type Journal Article
    ZDB-ID 807031-3
    ISSN 1791-7549 ; 0258-851X
    ISSN (online) 1791-7549
    ISSN 0258-851X
    DOI 10.21873/invivo.12619
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Comparison of the Usefulness of Computer-Assisted Three-Dimensional Analysis and Weight-Bearing Radiographs in Ankle Osteoarthritis.

    Lee, Si-Wook / Yon, Chang-Jin / Kim, Jae-Ho / Lee, Jung-Min / Lee, Jae-Ho / Heo, Yu-Ran

    Clinics in orthopedic surgery

    2024  Volume 16, Issue 1, Page(s) 141–148

    Abstract: Background: To evaluate the degree of deformation in patients with ankle osteoarthritis (OA), it is essential to measure the three-dimensional (3D), in other words, stereoscopic alignment of the ankle, subtalar, and foot arches. Generally, measurement ... ...

    Abstract Background: To evaluate the degree of deformation in patients with ankle osteoarthritis (OA), it is essential to measure the three-dimensional (3D), in other words, stereoscopic alignment of the ankle, subtalar, and foot arches. Generally, measurement of radiological parameters use two-dimensional (2D) anteroposterior and lateral radiographs in a weight-bearing state; however, computer-aided 3D analysis (Disior) using weight-bearing cone-beam computed tomography (CBCT) has recently been introduced.
    Methods: In this study, we compared the 2D human radiographic method with a stereoscopic image in patients with ankle arthritis. We enrolled 57 patients diagnosed with OA (28 left and 29 right) and obtained both standing radiographs and weight-bearing CBCT. Patients were divided by the Takakura stage. The interclass correlation coefficient (ICC) for each result was confirmed.
    Results: On the ICC between 2D radiographs and 3D analysis, the tibiotalar surface angle and lateral talo-1st metatarsal angle showed a good ICC grade (> 0.6), while other parameters did not have significant ICC results. Three-dimension was superior to radiographs in terms of statistical significance.
    Conclusions: We demonstrated that 2D and stereoscopic images are useful for the diagnosis of OA. Our study also confirmed that the radiographic features affected by ankle OA varied. However, according to the results, the typical radiography is not sufficient to diagnose and determine a treatment plan for ankle OA. Therefore, the method of using 3D images should be considered.
    MeSH term(s) Humans ; Ankle ; Radiography ; Ankle Joint/diagnostic imaging ; Osteoarthritis/diagnostic imaging ; Weight-Bearing ; Computers ; Reproducibility of Results
    Language English
    Publishing date 2024-01-15
    Publishing country Korea (South)
    Document type Journal Article
    ZDB-ID 2502788-8
    ISSN 2005-4408 ; 2005-291X
    ISSN (online) 2005-4408
    ISSN 2005-291X
    DOI 10.4055/cios23221
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  5. Article ; Online: Response: Acute Diffusion MRI Findings in Metabolic Encephalopathies are Diverse.

    Jeon, Se Jeong / Choi, See Sung / Kim, Ha Yon / Yu, In Kyu

    Korean journal of radiology

    2022  Volume 23, Issue 3, Page(s) 383–384

    MeSH term(s) Brain Diseases, Metabolic ; Diffusion Magnetic Resonance Imaging ; Humans
    Language English
    Publishing date 2022-02-25
    Publishing country Korea (South)
    Document type Letter ; Comment
    ZDB-ID 2046981-0
    ISSN 2005-8330 ; 1229-6929
    ISSN (online) 2005-8330
    ISSN 1229-6929
    DOI 10.3348/kjr.2021.0899
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Erratum: Acute Acquired Metabolic Encephalopathy Based on Diffusion MRI.

    Jeon, Se Jeong / Choi, See Sung / Kim, Ha Yon / Yu, In Kyu

    Korean journal of radiology

    2022  Volume 23, Issue 2, Page(s) 290

    Abstract: This corrects the article on p. 2034 in vol. 22, PMID: 34564957. ...

    Abstract This corrects the article on p. 2034 in vol. 22, PMID: 34564957.
    Language English
    Publishing date 2022-01-26
    Publishing country Korea (South)
    Document type Published Erratum
    ZDB-ID 2046981-0
    ISSN 2005-8330 ; 1229-6929
    ISSN (online) 2005-8330
    ISSN 1229-6929
    DOI 10.3348/kjr.2021.0952
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  7. Article ; Online: Comparison of TERT and 5-Hydroxymethylcytocine immunohistochemistry in various thyroid carcinomas.

    An, Hyeong Rok / Kim, Won Gu / Lee, Yu-Mi / Sung, Tae-Yon / Song, Dong Eun

    Annals of diagnostic pathology

    2024  Volume 71, Page(s) 152290

    Abstract: Telomerase reverse transcriptase (TERT) promoter mutation is associated with an aggressive clinical course in thyroid carcinomas. Therefore, detection of TERT promoter mutation is essential for proper patient management. 5-Hydroxymethylcytosine (5hmC) is ...

    Abstract Telomerase reverse transcriptase (TERT) promoter mutation is associated with an aggressive clinical course in thyroid carcinomas. Therefore, detection of TERT promoter mutation is essential for proper patient management. 5-Hydroxymethylcytosine (5hmC) is an epigenetic marker involved in the DNA demethylation pathway, and its loss has been observed in various tumors. Loss of 5hmC has also been reported in thyroid carcinomas and is presented as a possible predictive biomarker for TERT promoter mutation and worse prognosis. This study evaluated the expression of TERT and 5hmC by immunohistochemistry (IHC) in 105 patients (44 in the TERT mutant group and 61 in the TERT wild group) with various thyroid carcinomas. H-scores were calculated using an image analyzer. The median H-scores of TERT IHC were significantly higher in the TERT mutant group than in the TERT wild group (47.15 vs. 9.80). The sensitivity and specificity of TERT IHC for predicting TERT promoter mutations were 65.9 and 65.7 %, respectively. Regardless of TERT promoter mutation status, the 5hmC H-scores were markedly lower in all subtypes of thyroid carcinomas compared to those in their normal counterparts. Significant differences in 5hmC H-scores were observed between N0 and N1 in total thyroid carcinomas, but not within the papillary thyroid carcinoma subgroup. In conclusion, TERT and 5hmC IHC have limitations in predicting the presence of TERT promoter mutations. The expression of 5hmC was downregulated in various thyroid carcinomas compared to that in normal and benign lesions, but comprehensive further studies are required to elucidate the role of 5hmC in thyroid carcinomas.
    Language English
    Publishing date 2024-03-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1440011-x
    ISSN 1532-8198 ; 1092-9134
    ISSN (online) 1532-8198
    ISSN 1092-9134
    DOI 10.1016/j.anndiagpath.2024.152290
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  8. Article ; Online: Eflapegrastim's enhancement of efficacy compared with pegfilgrastim in neutropenic rats supports potential for same-day dosing.

    Barrett, John A / Choi, Jaehyuk / Lakshmikanthan, Sribalaji / Kim, Yu-Yon / Greene, Douglas / Kolli, Prasad / Song, Tae Hun / Choi, In Young / Kim, Young Hoon / Lebel, Francois

    Experimental hematology

    2020  Volume 92, Page(s) 51–61

    Abstract: Eflapegrastim (Rolontis) is a long-acting granulocyte colony-stimulating factor (G-CSF) with an IgG4 Fc fragment and short polyethylene glycol linker. Current G-CSF products are administered 24 hours after chemotherapy. The present study compares the ... ...

    Abstract Eflapegrastim (Rolontis) is a long-acting granulocyte colony-stimulating factor (G-CSF) with an IgG4 Fc fragment and short polyethylene glycol linker. Current G-CSF products are administered 24 hours after chemotherapy. The present study compares the duration of neutropenia (DN) with eflapegrastim or pegfilgrastim at 0, 2, 5, or 24 hours post chemotherapy. Eflapegrastim was evaluated by G-CSF receptor binding and bone marrow cell proliferation assays in vitro. Eflapegrastim-Fc component binding to Fcγ receptors C1q and FcRn was assessed by enzyme-linked immunosorbent assay. Neutropenia was induced in rats via intraperitoneal cyclophosphamide or docetaxel/cyclophosphamide. Rats received chemotherapy followed by vehicle, pegfilgrastim, or eflapegrastim at 2, 5, or 24 hours. The difference in DN after treatment was assessed. In vitro binding to G-CSF receptor of both agents was similar. Binding to FcRn and no binding to Fcγ receptors or C1q were observed with eflapegrastim. Studies in chemotherapy-induced neutropenic rats revealed shorter DN with eflapegrastim versus pegfilgrastim. Increased levels of G-CSF in serum and marrow were observed in groups treated with eflapegrastim versus those treated with pegfilgrastim. Although eflapegrastim and pegfilgrastim have similar in vitro binding affinity, the Fc fragment in eflapegrastim increases the uptake into bone marrow, resulting in increased therapeutic potential for chemotherapy-induced neutropenia. Eflapegrastim's greater marrow resident time provided a pharmacodynamic advantage over pegfilgrastim, translating into shortened duration of neutropenia. Our findings support eflapegrastim same-day administration with chemotherapy, warranting further evaluation in patients undergoing myelosuppressive chemotherapy.
    MeSH term(s) Animals ; Cyclophosphamide/adverse effects ; Cyclophosphamide/pharmacology ; Docetaxel/adverse effects ; Docetaxel/pharmacology ; Filgrastim/pharmacokinetics ; Filgrastim/pharmacology ; Histocompatibility Antigens Class I/blood ; Humans ; Male ; Mice ; Neutropenia/blood ; Neutropenia/chemically induced ; Neutropenia/drug therapy ; Neutropenia/pathology ; Polyethylene Glycols/pharmacokinetics ; Polyethylene Glycols/pharmacology ; Rats ; Rats, Sprague-Dawley ; Receptors, Fc/blood ; U937 Cells
    Chemical Substances Histocompatibility Antigens Class I ; Receptors, Fc ; Docetaxel (15H5577CQD) ; pegfilgrastim (3A58010674) ; Polyethylene Glycols (3WJQ0SDW1A) ; Cyclophosphamide (8N3DW7272P) ; Filgrastim (PVI5M0M1GW) ; Fc receptor, neonatal (TW3XAW0RCY)
    Language English
    Publishing date 2020-09-29
    Publishing country Netherlands
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 185107-x
    ISSN 1873-2399 ; 0531-5573 ; 0301-472X
    ISSN (online) 1873-2399
    ISSN 0531-5573 ; 0301-472X
    DOI 10.1016/j.exphem.2020.09.199
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  9. Article ; Online: Ethyl Acetate Fraction from a

    Kim, Yon-Suk / Lee, Eun-Bin / Yu, Ye-Ji / Kim, Ga-Won / Kim, Woo-Jung / Choi, Dong-Kug

    International journal of molecular sciences

    2023  Volume 25, Issue 1

    Abstract: The whitening effect of reducing skin pigmentation is one of the most important goals of cosmetics. The purpose of this study was to determine ... ...

    Abstract The whitening effect of reducing skin pigmentation is one of the most important goals of cosmetics. The purpose of this study was to determine whether
    MeSH term(s) Melanogenesis ; alpha-MSH/pharmacology ; Melanins ; Chromatography, Liquid ; Tandem Mass Spectrometry ; Monophenol Monooxygenase ; Bignoniaceae ; Cyclic AMP ; RNA, Messenger ; Plant Extracts/pharmacology ; Acetates
    Chemical Substances alpha-MSH (581-05-5) ; ethyl acetate (76845O8NMZ) ; Melanins ; Monophenol Monooxygenase (EC 1.14.18.1) ; Cyclic AMP (E0399OZS9N) ; RNA, Messenger ; Plant Extracts ; Acetates
    Language English
    Publishing date 2023-12-21
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms25010151
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  10. Article ; Online: Opioid use and subsequent delirium risk in patients with advanced cancer in palliative care: a multicenter registry study.

    Yoo, Shin Hye / Kang, Jiseung / Kim, Hyeon Jin / Lee, Si Won / Hong, Moonki / Jung, Eun Hee / Kim, Yu Jung / Yon, Dong Keon / Kang, Beodeul

    Scientific reports

    2024  Volume 14, Issue 1, Page(s) 6004

    Abstract: The prevalent use of opioids for pain management in patients with advanced cancer underscores the need for research on their neuropsychiatric impacts, particularly delirium. Therefore, we aimed to investigate the potential association between opioid use ... ...

    Abstract The prevalent use of opioids for pain management in patients with advanced cancer underscores the need for research on their neuropsychiatric impacts, particularly delirium. Therefore, we aimed to investigate the potential association between opioid use and the risk of delirium in patients with advanced cancer admitted to the acute palliative care unit. We conducted a retrospective observational study utilizing a multicenter, patient-based registry cohort by collecting the data from January 1, 2019, to December 31, 2020, in South Korea. All data regarding exposures, outcomes, and covariates were obtained through retrospective chart reviews by a team of specialized medical professionals with expertise in oncology. Full unmatched and 1:1 propensity-score matched cohorts were formed, and stratification analysis was conducted. The primary outcome, delirium, was defined and diagnosed by the DSM-IV. Of the 2,066 patients with advanced cancer, we identified 42.8% (mean [SD] age, 64.4 [13.3] years; 60.8% male) non-opioid users and 57.2% (62.8 [12.5] years; 55.9% male) opioid users, respectively. Opioid use was significantly associated with an increased occurrence of delirium in patients with advanced cancer (OR, 2.02 [95% CI 1.22-3.35]). The risk of delirium in patients with advanced cancer showed increasing trends in a dose-dependent manner. High-dose opioid users showed an increased risk of delirium in patients with advanced cancer compared to non-opioid users (low-dose user: OR, 2.21 [95% CI 1.27-3.84]; high-dose user: OR, 5.75 [95% CI 2.81-11.77]; ratio of OR, 2.60 [95% CI 1.05-6.44]). Patients with old age, male sex, absence of chemotherapy during hospitalization, and non-obese status were more susceptible to increased risk of delirium in patients with cancer. In this multicenter patient-based registry cohort study, we found a significant, dose-dependent association between opioid use and increased risk of delirium in patients with advanced cancer. We also identified specific patient groups more susceptible to delirium. These findings highlight the importance of opioid prescription in these patients with advanced cancer, balancing effective doses for pain management and adverse dose-inducing delirium.
    MeSH term(s) Humans ; Male ; Middle Aged ; Female ; Palliative Care ; Analgesics, Opioid/therapeutic use ; Retrospective Studies ; Cohort Studies ; Opioid-Related Disorders/drug therapy ; Neoplasms/drug therapy ; Delirium/etiology
    Chemical Substances Analgesics, Opioid
    Language English
    Publishing date 2024-03-12
    Publishing country England
    Document type Multicenter Study ; Observational Study ; Journal Article
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-024-56675-1
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