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  1. AU="Vachiraarunwong, Arpamas"
  2. AU="Mohammad-Najar, Narges"
  3. AU="Sarica, Kemal"
  4. AU="Lescure, Alain"
  5. AU="Darawan Rinchai"
  6. AU="Sarah K McKenzie"
  7. AU="Joseph Edgar Blais"
  8. AU="Garate, Jose Antonio"

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  1. Article ; Online: 2,4'-dihydroxy-6'-methoxy-3',5'-dimethylchalcone from Cleistocalyx nervosum var. paniala seeds attenuated the early stage of diethylnitrosamine and 1,2-dimethylhydrazine-induced colorectal carcinogenesis.

    Vachiraarunwong, Arpamas / Tuntiwechapikul, Wirote / Wongnoppavich, Ariyaphong / Meepowpan, Puttinan / Wongpoomchai, Rawiwan

    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

    2023  Volume 165, Page(s) 115221

    Abstract: Background: Dichloromethane extract of Cleistocalyx nervosum var. paniala seeds exhibited an anticarcinogenicity against chemically-induced the early stages of carcinogenesis in rats. This study aimed to identify anticarcinogenic compounds from C. ... ...

    Abstract Background: Dichloromethane extract of Cleistocalyx nervosum var. paniala seeds exhibited an anticarcinogenicity against chemically-induced the early stages of carcinogenesis in rats. This study aimed to identify anticarcinogenic compounds from C. nervosum seed extract (CSE).
    Methods: Salmonella mutation assay was performed to determine mutagenicity and antimutagenicity of partially purified and purified compounds of CSE. The anticarcinogenic enzyme-inducing activity was measured in Hepa1c1c7. Moreover, the anticancer potency was examined on various human cancer cell lines. The anticarcinogenicity of DMC was investigated using dual-organ carcinogenicity model. The number of preneoplastic lesions was evaluated in the liver and colon. The inhibitory mechanisms of DMC on liver- and colorectal carcinogenesis were investigated.
    Results: Six partially purified fractions (MK1 - MK6) and purified compounds, including 2,4'-dihydroxy-6'-methoxy-3',5'-dimethylchalcone (DMC) and hariganetin, were obtained from CSE. Among these fractions, MK4 and DMC presented the greatest antimutagenicity against indirect mutagens in bacterial model. Moreover, MK5 possessed an effective anticarcinogenic enzyme inducer in Hepa1c1c7. The MK4, DMC and CSE showed greater anticancer activity on all cell lines and exhibited the most effective toxicity on colon cancer cells. Furthermore, DMC inhibited the formation of colonic preneoplastic lesions in carcinogens-treated rats. It reduced PCNA-positive cells and frequency of BCAC in rat colon. DMC also enhanced the detoxifying enzyme, GST, in rat livers.
    Conclusions: DMC obtained from CSE may be a promising cancer chemopreventive compound of colorectal cancer process in rats. It could increase detoxifying enzymes and suppress the cell proliferation process resulting in prevention of post-initiation stage of colorectal carcinogenesis.
    MeSH term(s) Humans ; Rats ; Animals ; Syzygium ; Diethylnitrosamine ; 1,2-Dimethylhydrazine/toxicity ; Seeds ; Carcinogenesis ; Colorectal Neoplasms/chemically induced ; Colorectal Neoplasms/prevention & control
    Chemical Substances Diethylnitrosamine (3IQ78TTX1A) ; 1,2-Dimethylhydrazine (IX068S9745)
    Language English
    Publishing date 2023-07-28
    Publishing country France
    Document type Journal Article
    ZDB-ID 392415-4
    ISSN 1950-6007 ; 0753-3322 ; 0300-0893
    ISSN (online) 1950-6007
    ISSN 0753-3322 ; 0300-0893
    DOI 10.1016/j.biopha.2023.115221
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Early Detection of Hepatocarcinogenicity in Rats Using MRI with Ferric–Tannic Nanoparticles

    Intakhad, Jannarong / Vachiraarunwong, Arpamas / Sanit, Jantira / Kittilukkana, Aiyarin / Kongkarnka, Sarawut / Wongpoomchai, Rawiwan / Pilapong, Chalermchai

    Analytical Chemistry. 2023 June 26, v. 95, no. 27 p.10241-10248

    2023  

    Abstract: Herein, we present molecular nanoparticles of ferric–tannic complexes (so called ferric–tannic nanoparticles, FT NPs) used to enhance the MRI signal in the early stage of hepatocarcinoma. FT NPs were found to accumulate in the hepatic parenchyma without ... ...

    Abstract Herein, we present molecular nanoparticles of ferric–tannic complexes (so called ferric–tannic nanoparticles, FT NPs) used to enhance the MRI signal in the early stage of hepatocarcinoma. FT NPs were found to accumulate in the hepatic parenchyma without tumor nodules of Wistar rats in which hepatocarcinogenicity had been induced using diethylnitrosamine (DEN). The MRI enhancement and accumulation of FT NPs were clearly observed in the early phase of hepatocarcinogenicity, which was possibly modulated by various solute carrier family members present in the entire hepatic parenchyma of the DEN-induced rats. These findings suggest that MRI with FT NPs is promising for the assessment of the early stage of hepatocarcinoma.
    Keywords analytical chemistry ; diethylnitrosamine ; hepatoma ; nanoparticles ; solutes
    Language English
    Dates of publication 2023-0626
    Size p. 10241-10248.
    Publishing place American Chemical Society
    Document type Article ; Online
    ZDB-ID 1508-8
    ISSN 1520-6882 ; 0003-2700
    ISSN (online) 1520-6882
    ISSN 0003-2700
    DOI 10.1021/acs.analchem.3c00541
    Database NAL-Catalogue (AGRICOLA)

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  3. Article ; Online: Early Detection of Hepatocarcinogenicity in Rats Using MRI with Ferric-Tannic Nanoparticles.

    Intakhad, Jannarong / Vachiraarunwong, Arpamas / Sanit, Jantira / Kittilukkana, Aiyarin / Kongkarnka, Sarawut / Wongpoomchai, Rawiwan / Pilapong, Chalermchai

    Analytical chemistry

    2023  Volume 95, Issue 27, Page(s) 10241–10248

    Abstract: Herein, we present molecular nanoparticles of ferric-tannic complexes (so called ferric-tannic nanoparticles, FT NPs) used to enhance the MRI signal in the early stage of hepatocarcinoma. FT NPs were found to accumulate in the hepatic parenchyma without ... ...

    Abstract Herein, we present molecular nanoparticles of ferric-tannic complexes (so called ferric-tannic nanoparticles, FT NPs) used to enhance the MRI signal in the early stage of hepatocarcinoma. FT NPs were found to accumulate in the hepatic parenchyma without tumor nodules of Wistar rats in which hepatocarcinogenicity had been induced using diethylnitrosamine (DEN). The MRI enhancement and accumulation of FT NPs were clearly observed in the early phase of hepatocarcinogenicity, which was possibly modulated by various solute carrier family members present in the entire hepatic parenchyma of the DEN-induced rats. These findings suggest that MRI with FT NPs is promising for the assessment of the early stage of hepatocarcinoma.
    MeSH term(s) Rats ; Animals ; Liver Neoplasms/chemically induced ; Liver Neoplasms/diagnostic imaging ; Liver Neoplasms/pathology ; Carcinogenesis ; Rats, Wistar ; Carcinoma, Hepatocellular/chemically induced ; Carcinoma, Hepatocellular/diagnostic imaging ; Nanoparticles ; Magnetic Resonance Imaging ; Iron
    Chemical Substances Iron (E1UOL152H7)
    Language English
    Publishing date 2023-06-26
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1508-8
    ISSN 1520-6882 ; 0003-2700
    ISSN (online) 1520-6882
    ISSN 0003-2700
    DOI 10.1021/acs.analchem.3c00541
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Evaluation of the Mechanisms Involved in the Development of Bladder Toxicity following Exposure to Occupational Bladder Cancer Causative Chemicals Using DNA Adductome Analysis.

    Suzuki, Shugo / Gi, Min / Komiya, Masami / Obikane, Asuka / Vachiraarunwong, Arpamas / Fujioka, Masaki / Kakehashi, Anna / Totsuka, Yukari / Wanibuchi, Hideki

    Biomolecules

    2023  Volume 14, Issue 1

    Abstract: Occupational exposure to aromatic amines (AAs) is an important risk factor for urinary bladder cancer. This study aimed to evaluate the toxicity of AAs and analyze the carcinogenic mechanisms in rat bladder by comprehensive analysis of DNA adducts (DNA ... ...

    Abstract Occupational exposure to aromatic amines (AAs) is an important risk factor for urinary bladder cancer. This study aimed to evaluate the toxicity of AAs and analyze the carcinogenic mechanisms in rat bladder by comprehensive analysis of DNA adducts (DNA adductome). DNA was extracted from the bladder epithelia of rats treated with AAs, including acetoacet-
    MeSH term(s) Animals ; Rats ; Urinary Bladder ; DNA Adducts ; Urinary Bladder Neoplasms/chemically induced ; 8-Hydroxy-2'-Deoxyguanosine ; Amines ; Databases, Nucleic Acid ; Acetophenones ; Toluidines
    Chemical Substances 2-toluidine (B635MZ0ZLU) ; acetovanillone (B6J7B9UDTR) ; DNA Adducts ; 8-Hydroxy-2'-Deoxyguanosine (88847-89-6) ; Amines ; Acetophenones ; Toluidines
    Language English
    Publishing date 2023-12-26
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2701262-1
    ISSN 2218-273X ; 2218-273X
    ISSN (online) 2218-273X
    ISSN 2218-273X
    DOI 10.3390/biom14010036
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Characterizing the toxicological responses to inorganic arsenicals and their metabolites in immortalized human bladder epithelial cells.

    Vachiraarunwong, Arpamas / Gi, Min / Kiyono, Tohru / Suzuki, Shugo / Fujioka, Masaki / Qiu, Guiyu / Guo, Runjie / Yamamoto, Tomoki / Kakehashi, Anna / Shiota, Masayuki / Wanibuchi, Hideki

    Archives of toxicology

    2024  

    Abstract: Arsenic is highly toxic to the human bladder. In the present study, we established a human bladder epithelial cell line that closely mimics normal human bladder epithelial cells by immortalizing primary uroplakin 1B-positive human bladder epithelial ... ...

    Abstract Arsenic is highly toxic to the human bladder. In the present study, we established a human bladder epithelial cell line that closely mimics normal human bladder epithelial cells by immortalizing primary uroplakin 1B-positive human bladder epithelial cells with human telomerase reverse transcriptase (HBladEC-T). The uroplakin 1B-positive human bladder epithelial cell line was then used to evaluate the toxicity of seven arsenicals (iAs
    Language English
    Publishing date 2024-04-17
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 124992-7
    ISSN 1432-0738 ; 0340-5761
    ISSN (online) 1432-0738
    ISSN 0340-5761
    DOI 10.1007/s00204-024-03750-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: DNA Methylation Aberrations in Dimethylarsinic Acid-Induced Bladder Carcinogenesis.

    Yamamoto, Tomoki / Gi, Min / Yamashita, Satoshi / Suzuki, Shugo / Fujioka, Masaki / Vachiraarunwong, Arpamas / Guo, Runjie / Qiu, Guiyu / Kakehashi, Anna / Kato, Minoru / Uchida, Junji / Wanibuchi, Hideki

    Cancers

    2023  Volume 15, Issue 21

    Abstract: Arsenic is a known human urinary bladder carcinogen. While arsenic is known to cause aberrant DNA methylation, the mechanism of arsenic-triggered bladder carcinogenesis is not fully understood. The goal of this study was to identify aberrant DNA ... ...

    Abstract Arsenic is a known human urinary bladder carcinogen. While arsenic is known to cause aberrant DNA methylation, the mechanism of arsenic-triggered bladder carcinogenesis is not fully understood. The goal of this study was to identify aberrant DNA methylation in rat bladder urothelial carcinoma (UC) induced by dimethylarsinic acid (DMA
    Language English
    Publishing date 2023-11-03
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers15215274
    Database MEDical Literature Analysis and Retrieval System OnLINE

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