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All Journal Farmasains : Jurnal Farmasi dan Ilmu Kesehatan Jurnal Ilmiah Farmasi Statistika Jurnal Kedokteran Brawijaya Jurnal Teknosains Indonesian Journal of Cancer Chemoprevention Indonesian Journal of Pharmaceutical Science and Technology STOMATOGNATIC- Jurnal Kedokteran Gigi Indonesian Journal of Biotechnology Journal of Agromedicine and Medical Sciences Pharmacon Majalah Obat Tradisional Journal of Tropical Biodiversity and Biotechnology INDONESIAN JOURNAL OF PHARMACY JURNAL BIOLOGI INDONESIA Dental Journal (Majalah Kedokteran Gigi) The Indonesian Biomedical Journal Padjadjaran Journal of Dentistry Jurnal Kimia Terapan Indonesia JFIOnline YARSI Medical Journal Majalah Kesehatan Pharmamedika Pharmaceutical Sciences and Research (PSR)
Edy Meiyanto
Faculty Of Pharmacy, Universitas Gadjah Mada
Agriculture, Biological Sciences & Forestry Biochemistry, Genetics & Molecular Biology Chemical Engineering, Chemistry & Bioengineering Chemistry Civil Engineering, Building, Construction & Architecture Computer Science & IT Decision Sciences, Operations Research & Management Dentistry Economics, Econometrics & Finance Environmental Science Health Professions Immunology & microbiology Industrial & Manufacturing Engineering Materials Science & Nanotechnology Mathematics Mechanical Engineering Medicine & Pharmacology Public Health

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MEKANISME PENEKANAN EKSPRESI N-RAS EKSTRAK KULIT JERUK KEPROK (Citrus reticulata) SEBAGAI AGEN KEMOPREVENTIF N., Perdana Adhi; D., Andita Pra; P.K.W., Diah Ayu; Riyanto, Sugeng; Meiyanto, Edy
JFIOnline | Print ISSN 1412-1107 | e-ISSN 2355-696X Vol 4, No 3 (2009)
Publisher : Indonesian Research Gateway

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Abstract

One targeting point of cancer treatment, especially liver cancer is the suppression of N-Ras expression, inhibition of c-Src activity and CYP1A2 in the liver cells. The aim of the research in to explore the anticarcinogenesis effect of the ethanolic extract of C. reticulata peel through suppression of N-ras expression and the binding afinity and interaction of polimetoksiflavon compound found in the peel of Citrus Reticulata, namely tangeretin and nobiletin to the target protein using molecular docking. Geometry structure optimization tangeretin and nobiletin were done with the software Molecular Operating Environment (MOE) for Windows. The optimum structure conformation of tangeretin and nobiletin were approached using semiempirik AMBER99 method. The process of docking of the test compound to the bindingsite c-Src (PDB ID: 1FMK) and CYP1A2 (PDB ID: 1AE4) were done using the software Molecular Operating        Environment (MOE) for Windows in the conditions without water. From the docking process found that the lowest scoring value is tangeretin in conditions without water.  Docking Results of tangeretin compared with the experimental ligan in the target CYP1A2, shows the interaction of tangeretin stronger than the interaction of ligan an α-naphtoflavon. Meanwhile, the target protein, c-Src, interaction endogenous ligan (ATP) is much stronger than the interaction with the test compound and ligan comparison Imatinib. Therefore, it is estimated that the mechanism of liver cancer hepar inhibition in molecular docking is through CYP1A2 inhibition. ABSTRAK Salah satu titik tangkap pengobatan kanker khususnya kanker hepar adalah penekanan ekspresi N-Ras, penghambatan protein c-Src dan aktivitas CYP1A2 di hepar.  Penelitian ini bertujuan untuk mengetahui afinitas dan interaksi senyawa berkerangka polimetoksiflavon pada kulit jeruk keprok (Citrus reticulata) yaitu tangeretin dan nobiletin terhadap protein target tersebut menggunakan molecular docking. Optimasi geometri struktur tangeretin dan nobiletin dilakukan dengan piranti lunak Molecular Operating Environment for Windows.  Konformasi optimum tangeretin dan nobiletin dihasilkan menggunakan metode semiempirik AMBER99. Kemudian dilakukan proses docking senyawa uji dengan bindingsite c-Src (PDB ID : 1FMK) dan CYP1A2 (PDB ID : 1AE4) menggunakan piranti lunak Molecular Operating Environment for Windows dalam kondisi tanpa air. Dari hasil yang diperoleh dapat diperkirakan bahwa mekanisme penghambatan kanker hepar secara docking molekuler adalah melalui penghambatan CYP1A2
PENTAGAMAVUNON-1 MENGHAMBAT SIKLUS SEL T47D TERINDUKSI CASPASE INHIBITOR Z-VAD-Fmk PADA FASE G2-M Da’i, Muhammad; A.M., Supardjan; Jenie, Umar Anggara; M, Kawaichi; Meiyanto, Edy
JFIOnline | Print ISSN 1412-1107 | e-ISSN 2355-696X Vol 5, No 4 (2011)
Publisher : Indonesian Research Gateway

Show Abstract | Download Original | Original Source | Check in Google Scholar

Abstract

Previous experiment indicated Curcumin’s analogue Pentagamavunon-1 (2,5-bis(41-hidroxy-31,51-dimethyl)-benzilidine-cyclopentanone) has inhibitory activity on T47D cell proliferation through induction of apoptosis and cell cycle arrest at G2-M phase. This research was conducted to observe the relationship between the induction of apoptosis and inhibition of cell cycle in T47D cells induced by Pentagamavunon-1 (PGV-1). The T47D cells were treated with 2.5 PGV-1 mM; Z-VAD-Fmk 2.5 mM; (Z-VAD-Fmk 2.5 mM+PGV-1 2.5 mM). Kinetics of cell proliferation was observed with flowcytometer analysis, molecular expression was observed with Western blot methods. The results showed induction of PGV-1 and Z-VAD-Fmk stimulate the accumulation of cells in G2-M phase (39.28%), did not differ significantly with cells that  induced by PGV-1 only (34.19%). Molecular analysis showed that treatment with (PGV-1+Z-VAD-Fmk) could prevent apoptosis through inhibition of activation of Caspase-3, increased the expression of p21 and activated Cdc-2. Overall the study showed inhibition of cell cycle at G2M phase by PGV-1 compound is not affected by the activation of caspase-3. ABSTRAK Analog kurkumin Pentagamavunon-1  (2,5-bis(41-hidroksi-31,51-dimetil)-benzilidinsiklo-pentanon) telah diteliti dapat menghambat proliferasi sel melalui mekanisme induksi apoptosis dan cell cycle arrest pada fase G2-M. Penelitian ini dilakukan untuk mengamati keterkaitan antara proses induksi apoptosis dan penghambatan siklus sel pada sel T47D yang diinduksi senyawa Pentagamavunon-1 (PGV-1). Sel T47D diberi perlakuan PGV-1 2,5 mM; Z-VAD-Fmk 2,5 mM dan (Z-VAD-Fmk 2,5 mM+PGV-1 2,5 mM). Kinetika proliferasi sel diamati dengan analisis flowcytometric, ekspresi molekuler diamati dengan metode Western blot. Hasil pengamatan menunjukkan induksi (PGV-1+Z-VAD-Fmk) memacu akumulasi sel pada fase G2-M (39,28%) tidak berbeda signifikan dengan sel yang hanya diinduksi PGV-1 (34,19%). Pengamatan molekuler menunjukkan perlakuan (PGV-1+Z-VAD-Fmk) mencegah terjadinya apoptosis melalui penghambatan aktivasi Caspase-3. Secara keseluruhan penelitian menunjukkan penghambatan siklus sel pada fase G2-M oleh senyawa PGV-1 tidak tergantung oleh aktivasi Caspase-3.
PENGARUH EKSTRAK RIMPANG TEMU PUTIH (Curcuma zedoaria Rosc.) TERHADAP KARSINOGENESIS PARU YANG DIINDUKSI OLEH BENZO[]PIREN Murwanti, Retno; Meiyanto, Edy; Nurrochmad, Arief; Alexxander, .
JFIOnline | Print ISSN 1412-1107 | e-ISSN 2355-696X Vol 3, No 2 (2006)
Publisher : Indonesian Research Gateway

Show Abstract | Download Original | Original Source | Check in Google Scholar

Abstract

This experiment was aimed to investigate the influence of Curcuma zedoaria Rosc. ethanol extract on the growth of benzo[a]pyrene-induced lung tumor in male Balb/c mice. New born miced were induced with 0,2 mmol, 0,4 mmol, and 0,8 mmol benzo[a]pyrene intraperitoneally at day 1, 8, and 15 after born. On day 25 after born, the male mice were distributed into 5 groups. Group 1, 2 and 3 were treated with Curcuma zedoaria Rosc. ethanol extract consecutively 250 mg/kgBW, 500 mg/kgBW and 750 mg/kgBW. Group 4 was treated with DMSO (solvent) and group 5 was B[a]P induced tumor positive control.  Mice were sacrificed at 4 month age, and lung were collected for examination of tumor nodules macroscopic and microscopically. Intensity of carcinogenicity was expressed as number of  tumor bearing mice in each group, and number of of tumor nodules per mouse lung. From the result it was concluded that  Curcuma zedoaria Rosc. ethanol extract dose 250-750 mg/kgBW can inhibit the growth of lung tumor in male mice up to 18,75%. ABSTRAK Penelitian ini bertujuan untuk mengetahui pengaruh ekstrak etanol rimpang temu putih terhadap pertumbuhan  tumor paru pada mencit jantan galur Balb/c yang diinduksi benzo[a]piren. Anak mencit yang baru lahir diinduksi secara intraperitoneal dengan benzo[a]piren pada hari ke-1, ke-8, dan ke-15 setelah kelahiran dengan dosis masing-masing sebesar 0,2 mmol, o,4 mmol, dan 0,8 mmol. Pada hari ke-25 setelah kelahiran, mencit jantan dibagi menjadi 5 kelompok, kelompok pertama sampai ke-3 diberi ekstrak etanol rimpang temu putih dengan dosis 250 mg/kgBB, 500 mg/kgBB dan 750 mg/kgBB, kelompok  ke-4 diberi pelarut DMSO dan kelompok ke-5 sebagai kelompok kontrol positif kanker B[a]P. Mencit dikorbanan pada umur 4 bulan dan diambil organ paru, untuk diamati adanya nodul tumor secara makroskopis dan mokroskopis. Intensitas karsinogenesitas dinyatakan sebagai jumlah mencit yang terkena tumor paru dalam setiap kelompok, dan jumlah tumor per mencit dalam setiap organ paru. Analisis statistik yang digunakan adalah analisis Non parametrik Test (Kruskal-Wallis Test) dan diteruskan dengan Mann-Whitney Test. Dari penelitian ini diambil kesimpulan bahwa ekstrak etanol rimpang temu putih dengan dosis 250 mg/kgBB, 500 mg/kgBB, dan dosis 750 mg/kgBB mampu menghambat pertumbuhan tumor paru pada mencit jantan pada fase post inisiasi dengan prosentase penghambatan berturut-turut 28,5%, 83,5%, dan 18,75%.
EFEK SITOTOKSIK EKSTRAK TANAMAN KELADI TIKUS (Typhonium divaricatum (L.) TERHADAP SEL HeLa Da’i, Muhammad; Fiveri, Anis; Meiyanto, Edy
JFIOnline | Print ISSN 1412-1107 | e-ISSN 2355-696X Vol 3, No 4 (2007)
Publisher : Indonesian Research Gateway

Show Abstract | Download Original | Original Source | Check in Google Scholar

Abstract

Cervic cancer is the most cancer that suffered by women in the world include in Indonesia. The main purposes of this experiment is to explore the Indonesian plan to find new anticancer agent. This experiment exhibit the cytotoxic effect of (Typhonium divaricatum (L.) Decne) on HeLa cells line. This experiment also directed to know the corelation phenolic content with the cytotoxic effect of extracts Typhonium divaricatum. The result indicated ethyl acetate extract had the best potency as cytotoxic agent compared with ethanol and cloroform extract based on MTT method. The IC50 value of ethil acetate extract was 147,77 μg/ml, chloroform extract was 903,44 μg/ml (based on the extrapolation). Ethanol extract was not resulted the IC50 value. Phenol content in each extracts was resulted by Folin-Ciocalteu method. Total phenol content of ethyl acetate, ethanol and chloroform extracts were 13.154; 12.028; 2.872 mg/g extract respectively. Those results indicate there is no corelation between total phenol content and cytotoxic effect direcly of each extracts. ABSTRAK Kanker leher rahim adalah kanker yang banyak diderita wanita diseluruh dunia, termasuk di Indonesia. Selama ini terapi kanker dengan kemoterapi belum memperoleh hasil yang memuaskan. Penelitian ini dilakukan untuk mendapatkan bahan obat dari alam sebagai antikanker dari tanaman Indonesia. Penelitian ini dilakukan untuk menentukan efek sitotoksik keladi tikus (Typhonium divaricatum (L.) Decne) pada sel kanker leher rahim (sel HeLa) dan diarahkan pula untuk mengetahui korelasi kandungan senyawa fenolik terhadap potensi sitotoksisitas ekstrak tanaman keladi tikus. Hasil uji sitotoksik terhadap sel HeLa, ekstrak etil asetat memiliki efek sitotoksik terbesar terhadap sel HeLa dibanding ekstrak kloroform dan etanol. Nilai IC50 ekstrak etil asetat adalah 147,77 μg/ml, kloroform sebesar 903,44 μg/ml (hasil ekstrapolasi), sedangkan harga IC50 ekstrak etanol tidak dapat ditentukan. Penetapan kadar fenol total dalam masing-masing ekstrak ekstrak tanaman keladi tikus diperoleh dengan penyari etil asetat (13,154 mg/g ekstrak) > etanol (12,028 mg/g ekstrak) > kloroform (2,872 mg/g ekstrak). Hasil-hasil tersebut menunjukkan kandungan senyawa fenolik bukan merupakan penanda utama potensi sitotoksik suatu ekstrak.
PENTAGAMAVUNON-1 MENGHAMBAT SIKLUS SEL T47D TERINDUKSI CASPASE INHIBITOR Z-VAD-Fmk PADA FASE G2-M Daâ??i, Muhammad; A.M., Supardjan; Jenie, Umar Anggara; M, Kawaichi; Meiyanto, Edy
Jurnal Farmasi Indonesia Vol 5, No 4 (2011)
Publisher : Jurnal Farmasi Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.35617/jfi.v5i4.54

Abstract

Previous experiment indicated Curcuminâ??s analogue Pentagamavunon-1 (2,5-bis(41-hidroxy-31,51-dimethyl)-benzilidine-cyclopentanone) has inhibitory activity on T47D cell proliferation through induction of apoptosis and cell cycle arrest at G2-M phase. This research was conducted to observe the relationship between the induction of apoptosis and inhibition of cell cycle in T47D cells induced by Pentagamavunon-1 (PGV-1). The T47D cells were treated with 2.5 PGV-1 mM; Z-VAD-Fmk 2.5 mM; (Z-VAD-Fmk 2.5 mM+PGV-1 2.5 mM). Kinetics of cell proliferation was observed with flowcytometer analysis, molecular expression was observed with Western blot methods. The results showed induction of PGV-1 and Z-VAD-Fmk stimulate the accumulation of cells in G2-M phase (39.28%), did not differ significantly with cells that  induced by PGV-1 only (34.19%). Molecular analysis showed that treatment with (PGV-1+Z-VAD-Fmk) could prevent apoptosis through inhibition of activation of Caspase-3, increased the expression of p21 and activated Cdc-2. Overall the study showed inhibition of cell cycle at G2M phase by PGV-1 compound is not affected by the activation of caspase-3. ABSTRAK Analog kurkumin Pentagamavunon-1  (2,5-bis(41-hidroksi-31,51-dimetil)-benzilidinsiklo-pentanon) telah diteliti dapat menghambat proliferasi sel melalui mekanisme induksi apoptosis dan cell cycle arrest pada fase G2-M. Penelitian ini dilakukan untuk mengamati keterkaitan antara proses induksi apoptosis dan penghambatan siklus sel pada sel T47D yang diinduksi senyawa Pentagamavunon-1 (PGV-1). Sel T47D diberi perlakuan PGV-1 2,5 mM; Z-VAD-Fmk 2,5 mM dan (Z-VAD-Fmk 2,5 mM+PGV-1 2,5 mM). Kinetika proliferasi sel diamati dengan analisis flowcytometric, ekspresi molekuler diamati dengan metode Western blot. Hasil pengamatan menunjukkan induksi (PGV-1+Z-VAD-Fmk) memacu akumulasi sel pada fase G2-M (39,28%) tidak berbeda signifikan dengan sel yang hanya diinduksi PGV-1 (34,19%). Pengamatan molekuler menunjukkan perlakuan (PGV-1+Z-VAD-Fmk) mencegah terjadinya apoptosis melalui penghambatan aktivasi Caspase-3. Secara keseluruhan penelitian menunjukkan penghambatan siklus sel pada fase G2-M oleh senyawa PGV-1 tidak tergantung oleh aktivasi Caspase-3.
EFEK SITOTOKSIK EKSTRAK TANAMAN KELADI TIKUS (Typhonium divaricatum (L.) TERHADAP SEL HeLa Daâ??i, Muhammad; Fiveri, Anis; Meiyanto, Edy
Jurnal Farmasi Indonesia Vol 3, No 4 (2007)
Publisher : Jurnal Farmasi Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.35617/jfi.v3i4.86

Abstract

Cervic cancer is the most cancer that suffered by women in the world include in Indonesia. The main purposes of this experiment is to explore the Indonesian plan to find new anticancer agent. This experiment exhibit the cytotoxic effect of (Typhonium divaricatum (L.) Decne) on HeLa cells line. This experiment also directed to know the corelation phenolic content with the cytotoxic effect of extracts Typhonium divaricatum. The result indicated ethyl acetate extract had the best potency as cytotoxic agent compared with ethanol and cloroform extract based on MTT method. The IC50 value of ethil acetate extract was 147,77 μg/ml, chloroform extract was 903,44 μg/ml (based on the extrapolation). Ethanol extract was not resulted the IC50 value. Phenol content in each extracts was resulted by Folin-Ciocalteu method. Total phenol content of ethyl acetate, ethanol and chloroform extracts were 13.154; 12.028; 2.872 mg/g extract respectively. Those results indicate there is no corelation between total phenol content and cytotoxic effect direcly of each extracts. ABSTRAK Kanker leher rahim adalah kanker yang banyak diderita wanita diseluruh dunia, termasuk di Indonesia. Selama ini terapi kanker dengan kemoterapi belum memperoleh hasil yang memuaskan. Penelitian ini dilakukan untuk mendapatkan bahan obat dari alam sebagai antikanker dari tanaman Indonesia. Penelitian ini dilakukan untuk menentukan efek sitotoksik keladi tikus (Typhonium divaricatum (L.) Decne) pada sel kanker leher rahim (sel HeLa) dan diarahkan pula untuk mengetahui korelasi kandungan senyawa fenolik terhadap potensi sitotoksisitas ekstrak tanaman keladi tikus. Hasil uji sitotoksik terhadap sel HeLa, ekstrak etil asetat memiliki efek sitotoksik terbesar terhadap sel HeLa dibanding ekstrak kloroform dan etanol. Nilai IC50 ekstrak etil asetat adalah 147,77 μg/ml, kloroform sebesar 903,44 μg/ml (hasil ekstrapolasi), sedangkan harga IC50 ekstrak etanol tidak dapat ditentukan. Penetapan kadar fenol total dalam masing-masing ekstrak ekstrak tanaman keladi tikus diperoleh dengan penyari etil asetat (13,154 mg/g ekstrak) > etanol (12,028 mg/g ekstrak) > kloroform (2,872 mg/g ekstrak). Hasil-hasil tersebut menunjukkan kandungan senyawa fenolik bukan merupakan penanda utama potensi sitotoksik suatu ekstrak.
MEKANISME PENEKANAN EKSPRESI N-RAS EKSTRAK KULIT JERUK KEPROK (Citrus reticulata) SEBAGAI AGEN KEMOPREVENTIF N., Perdana Adhi; D., Andita Pra; P.K.W., Diah Ayu; Riyanto, Sugeng; Meiyanto, Edy
Jurnal Farmasi Indonesia Vol 4, No 3 (2009)
Publisher : Jurnal Farmasi Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.35617/jfi.v4i3.17

Abstract

One targeting point of cancer treatment, especially liver cancer is the suppression of N-Ras expression, inhibition of c-Src activity and CYP1A2 in the liver cells. The aim of the research in to explore the anticarcinogenesis effect of the ethanolic extract of C. reticulata peel through suppression of N-ras expression and the binding afinity and interaction of polimetoksiflavon compound found in the peel of Citrus Reticulata, namely tangeretin and nobiletin to the target protein using molecular docking. Geometry structure optimization tangeretin and nobiletin were done with the software Molecular Operating Environment (MOE) for Windows. The optimum structure conformation of tangeretin and nobiletin were approached using semiempirik AMBER99 method. The process of docking of the test compound to the bindingsite c-Src (PDB ID: 1FMK) and CYP1A2 (PDB ID: 1AE4) were done using the software Molecular Operating        Environment (MOE) for Windows in the conditions without water. From the docking process found that the lowest scoring value is tangeretin in conditions without water.  Docking Results of tangeretin compared with the experimental ligan in the target CYP1A2, shows the interaction of tangeretin stronger than the interaction of ligan an α-naphtoflavon. Meanwhile, the target protein, c-Src, interaction endogenous ligan (ATP) is much stronger than the interaction with the test compound and ligan comparison Imatinib. Therefore, it is estimated that the mechanism of liver cancer hepar inhibition in molecular docking is through CYP1A2 inhibition. ABSTRAK Salah satu titik tangkap pengobatan kanker khususnya kanker hepar adalah penekanan ekspresi N-Ras, penghambatan protein c-Src dan aktivitas CYP1A2 di hepar.  Penelitian ini bertujuan untuk mengetahui afinitas dan interaksi senyawa berkerangka polimetoksiflavon pada kulit jeruk keprok (Citrus reticulata) yaitu tangeretin dan nobiletin terhadap protein target tersebut menggunakan molecular docking. Optimasi geometri struktur tangeretin dan nobiletin dilakukan dengan piranti lunak Molecular Operating Environment for Windows.  Konformasi optimum tangeretin dan nobiletin dihasilkan menggunakan metode semiempirik AMBER99. Kemudian dilakukan proses docking senyawa uji dengan bindingsite c-Src (PDB ID : 1FMK) dan CYP1A2 (PDB ID : 1AE4) menggunakan piranti lunak Molecular Operating Environment for Windows dalam kondisi tanpa air. Dari hasil yang diperoleh dapat diperkirakan bahwa mekanisme penghambatan kanker hepar secara docking molekuler adalah melalui penghambatan CYP1A2
PENGARUH EKSTRAK RIMPANG TEMU PUTIH (Curcuma zedoaria Rosc.) TERHADAP KARSINOGENESIS PARU YANG DIINDUKSI OLEH BENZO[]PIREN Murwanti, Retno; Meiyanto, Edy; Nurrochmad, Arief; Alexxander, .
Jurnal Farmasi Indonesia Vol 3, No 2 (2006)
Publisher : Jurnal Farmasi Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.35617/jfi.v3i2.71

Abstract

This experiment was aimed to investigate the influence of Curcuma zedoaria Rosc. ethanol extract on the growth of benzo[a]pyrene-induced lung tumor in male Balb/c mice. New born miced were induced with 0,2 mmol, 0,4 mmol, and 0,8 mmol benzo[a]pyrene intraperitoneally at day 1, 8, and 15 after born. On day 25 after born, the male mice were distributed into 5 groups. Group 1, 2 and 3 were treated with Curcuma zedoaria Rosc. ethanol extract consecutively 250 mg/kgBW, 500 mg/kgBW and 750 mg/kgBW. Group 4 was treated with DMSO (solvent) and group 5 was B[a]P induced tumor positive control.  Mice were sacrificed at 4 month age, and lung were collected for examination of tumor nodules macroscopic and microscopically. Intensity of carcinogenicity was expressed as number of  tumor bearing mice in each group, and number of of tumor nodules per mouse lung. From the result it was concluded that  Curcuma zedoaria Rosc. ethanol extract dose 250-750 mg/kgBW can inhibit the growth of lung tumor in male mice up to 18,75%. ABSTRAK Penelitian ini bertujuan untuk mengetahui pengaruh ekstrak etanol rimpang temu putih terhadap pertumbuhan  tumor paru pada mencit jantan galur Balb/c yang diinduksi benzo[a]piren. Anak mencit yang baru lahir diinduksi secara intraperitoneal dengan benzo[a]piren pada hari ke-1, ke-8, dan ke-15 setelah kelahiran dengan dosis masing-masing sebesar 0,2 mmol, o,4 mmol, dan 0,8 mmol. Pada hari ke-25 setelah kelahiran, mencit jantan dibagi menjadi 5 kelompok, kelompok pertama sampai ke-3 diberi ekstrak etanol rimpang temu putih dengan dosis 250 mg/kgBB, 500 mg/kgBB dan 750 mg/kgBB, kelompok  ke-4 diberi pelarut DMSO dan kelompok ke-5 sebagai kelompok kontrol positif kanker B[a]P. Mencit dikorbanan pada umur 4 bulan dan diambil organ paru, untuk diamati adanya nodul tumor secara makroskopis dan mokroskopis. Intensitas karsinogenesitas dinyatakan sebagai jumlah mencit yang terkena tumor paru dalam setiap kelompok, dan jumlah tumor per mencit dalam setiap organ paru. Analisis statistik yang digunakan adalah analisis Non parametrik Test (Kruskal-Wallis Test) dan diteruskan dengan Mann-Whitney Test. Dari penelitian ini diambil kesimpulan bahwa ekstrak etanol rimpang temu putih dengan dosis 250 mg/kgBB, 500 mg/kgBB, dan dosis 750 mg/kgBB mampu menghambat pertumbuhan tumor paru pada mencit jantan pada fase post inisiasi dengan prosentase penghambatan berturut-turut 28,5%, 83,5%, dan 18,75%.
Co-Authors . Anindyajati . Larasati . Sugiyanto Adam Hermawan Adam Hermawan Adisusilo, Midori Rahmadhany Putri Aditya Fitriasari Aditya Fitriasari Agung Endro Nugroho Agusta Fauzi, Ilham Agustina Setiawati Ainun Wulandari Alexxander, . Alexxander, . Ameilinda Monikawati Ameilinda Monikawati Andita Pra Darma Andita Pra Darma Andriyani, Rina Angelina, Marissa Angraini, Sonia Meta Anif Nur Artanti, Anif Nur Ardriyanto, Maria Indra Arief Nurrochmad Arief Rahman Hakim Asih Triastuti Astrid Ayu Maruti Aulia Katarina Aulia Rahman, Faaza Ayu Maruti, Astrid B. Sudarto Banun Kusumawardani Chio Oka, Chio D., Andita Pra D., Andita Pra Da'i, Muhammad Da’i, Muhammad Dewi Arum Sekti, Dewi Arum Dewi Pamungkas Putri, Dyaningtyas Dewi Pratiwi Dini Maharani Djaswadi Dasuki Dwi Ana Nawangsari Dwi Ana Nawangsari, Dwi Ana Dwi Merry Christmarini Robin Dwi Nurahmanto Dyaningtyas D. P. Putri Dyaningtyas Dewi Putri Pamungkas Effendi, Fatiha Citra Endah Puji Septisetyani, Endah Puji Endah Puspitasari Endang Lukitaningsih Endang Purwaningsih Erlina Rivanti Erna Prawita Setyowati Esti, Yuni Fajar Fany Mutia Cahyani Farmasyanti, Cendrawasih Andusyana Feby Handoko, Fransiscus Fikri Amalia Fina Aryani Goenadi Fina Aryani Goenadi, Fina Aryani Fitria Rahmi Fiveri, Anis Fiveri, Anis Fortunella Tjondro Handayani, Sri Handayani, Sri Hanifa, Mila Hapsari, Novia Permata Hargiani, Fransisca Xaveria Harsan, Hayfa Salsabila Hastuti, Hanaan Emilia Adi Hendra Kurniawan Maury Hendri Wasito Heni Susilowati Herwandhani Putri Herwandhani Putri Ibrahim Arifin Ida Ayu Putu Sri Widnyani Ika Nurzijah Ika Rahmawati Sutejo Ikawati, Muthi' Ilham Agusta Fauzi Ilham Agusta Fauzi Imono Argo Donatus, Imono Argo Indrasetiawan, Puguh Indri Kusharyanti Inna Armandani, Inna Inna Armandari Iwan Sahrial Hamid JAKA WIDADA Jauhari, Fahmi Ihsanuddin Jenie, Riris Istighfari Jenie, Riris Istighfari Juni Ekowati Kadarsih Soejono, Sri Kadarsih Soejono, Sri Kartika Dyah Palupi Kartika Dyah Palupi Kato, Jun-Ya Kawai, Taro Kholid Alfan Nur Kholid Alfan Nur Komang Alit Paramitasari Kuijpers-Jagtman, Anne Marie Kumara, Dennaya Laras Widawaty Putri Lestari, Dinda Luthfia Indriyani M, Kawaichi M, Kawaichi Mae Sri Hartati Wahyuningsih Maran, Gergorius Gena Marcellino Rudyanto Maria Dwi Supriyati Maria Dwi Supriyati, Maria Dwi Masashi Kawaichi Masashi Kawaichi, Masashi Muflikhasari, Haruma Anggraini Muhammad Da'i Muhammad Fithrul Mubarok, Muhammad Fithrul Muthi Ikawati N., Perdana Adhi N., Perdana Adhi Nabila, Klarissa Nanda Resa Pratama Niken Nur W, Niken Novi Hastuti, Novi Novianti, Metta Novitasari, Dhania Nugraheni, Nadzifa Nunuk Aries Nurulita Nunuk Purwanti Nurma Sabila Nurrachma, Marsya Yonna P.K.W., Diah Ayu P.K.W., Diah Ayu Perdana Adhi Nugroho Perdana Adhi Nugroho Prasetyaningrum, Pekik Wiji Pudjono Pudjono Putri, Amaliya Permata Putri, Herwandhani Putri, Nindya Budiana R A Susidarti Raditya Prima Istiaji Rahmah, Inggita Hasi Rahman, Faaza Aulia Rahmawati, Desty Restia Rahmi Khamsita Ramadani, Ratna Dwi Ratih Hardika Pratama Ratna Asmah Susidarti Ratna Asmah Susidarti Retno Ardhani Retno Murwanti Rifai, Fauziah Novita Putri Riris I Jenie Riris I Jenie, Riris I Riris Istighfari Jenie Riris Istighfari Jenie Riris Istighfari Jenie Risdian, Chandra Rita Riata Rohmad Yudi Utomo Rohmad Yudi Utomo Rosa Adelina Rosana Anna Ashari Rosana Anna Ashari, Rosana Anna Rosye H.R. Tanjung Rul Afiyah Syarif Rumiyati, Rumiyati Salsabila, Irfani Aura Santoso, Christopher Filando Sari Haryanti Sari Haryanti Sarmoko Sarmoko Sendy Junedi Sendy Junedy, Sendy Shigeru Sasaki Sismindari . Sitarina Widyarini Sofa Farida Sri . Handayani Sri Handayani Sri Kadarsih Soejono Sri Kasianningsih Sri Susilowati Sri Tasminatun Sugeng Riyanto Sugiyanto . Sugiyanto . Sukardiman Supardjan A. M. Supardjan A.M., Supardjan Supardjan AM Supardjan AM, Supardjan Susi Ari Kristina Tutuk Budiati Udin, Zalinar Umar A. Jenie Umar Anggara Jenie Umar Anggara Jenie Umar Anggara Jenie Widayanti, Wasita Rachma Yundari, Yundari Yurista Gilang Yurista Gilang Ikhtiarsyah Yuyun Farida Yuyun Farida, Yuyun Zufairo, Shofa Khamdanatuz Zulfin, Ummi Maryam