Anticancer activity of Aristolochia ringens Vahl. (Aristolochiaceae)

Cancer is a leading cause of death worldwide and sustained focus is on the discovery and development of newer and better tolerated anticancer drugs especially from plants. The sulforhodamine B (SRB) in vitro cytotoxicity assay, sarcoma-180 (S-180) ascites and solid tumor, and L1210 lymphoid leukemia...

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Main Authors: Abidemi James Akindele, Zahoor Wani, Girish Mahajan, Sadhana Sharma, Flora Ruth Aigbe, Naresh Satti, Olufunmilayo Olaide Adeyemi, Dilip Manikrao Mondhe
Format: Article
Language:English
Published: Elsevier 2015-01-01
Series:Journal of Traditional and Complementary Medicine
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2225411014000091
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spelling doaj-dd5336e6954c4448b3464c14720386062020-11-24T23:37:48ZengElsevierJournal of Traditional and Complementary Medicine2225-41102015-01-0151354110.1016/j.jtcme.2014.05.001Anticancer activity of Aristolochia ringens Vahl. (Aristolochiaceae)Abidemi James Akindele0Zahoor Wani1Girish Mahajan2Sadhana Sharma3Flora Ruth Aigbe4Naresh Satti5Olufunmilayo Olaide Adeyemi6Dilip Manikrao Mondhe7Cancer Pharmacology Division, Indian Institute of Integrative Medicine, Council of Scientific and Industrial Research, Jammu, Jammu and Kashmir, IndiaCancer Pharmacology Division, Indian Institute of Integrative Medicine, Council of Scientific and Industrial Research, Jammu, Jammu and Kashmir, IndiaCancer Pharmacology Division, Indian Institute of Integrative Medicine, Council of Scientific and Industrial Research, Jammu, Jammu and Kashmir, IndiaCancer Pharmacology Division, Indian Institute of Integrative Medicine, Council of Scientific and Industrial Research, Jammu, Jammu and Kashmir, IndiaDepartment of Pharmacology, Therapeutics and Toxicology, Faculty of Basic Medical Sciences, College of Medicine, University of Lagos, Lagos, NigeriaNatural Products Chemistry Division, Indian Institute of Integrative Medicine, Council of Scientific and Industrial Research, Jammu, Jammu and Kashmir, IndiaDepartment of Pharmacology, Therapeutics and Toxicology, Faculty of Basic Medical Sciences, College of Medicine, University of Lagos, Lagos, NigeriaCancer Pharmacology Division, Indian Institute of Integrative Medicine, Council of Scientific and Industrial Research, Jammu, Jammu and Kashmir, IndiaCancer is a leading cause of death worldwide and sustained focus is on the discovery and development of newer and better tolerated anticancer drugs especially from plants. The sulforhodamine B (SRB) in vitro cytotoxicity assay, sarcoma-180 (S-180) ascites and solid tumor, and L1210 lymphoid leukemia in vivo models were used to investigate the anticancer activity of root extracts of Aristolochia ringens Vahl. (Aristolochiaceae; 馬兜鈴 mǎ dōu líng). AR-A001 (IC50 values of 20 μg/mL, 22 μg/mL, 3 μg/mL, and 24 μg/mL for A549, HCT-116, PC3, and THP-1 cell lines, respectively), and AR-A004 (IC50 values of 26 μg/mL, 19.5 μg/mL, 12 μg/mL, 28 μg/mL, 30 μg/mL, and 22 μg/mL for A549, HCT-116, PC3, A431, HeLa, and THP-1, respectively), were observed to be significantly active in vitro. Potency was highest with AR-A001 and AR-A004 for PC3 with IC50 values of 3 μg/mL and 12 μg/mL, respectively. AR-A001 and AR-A004 produced significant (p < 0.05–0.001) dose-dependent inhibition of tumor growth in the S-180 ascites model with peak effects produced at the highest dose of 120 mg/kg. Inhibition values were 79.51% and 89.98% for AR-A001 and AR-A004, respectively. In the S-180 solid tumor model, the inhibition of tumor growth was 29.45% and 50.50% for AR-A001 (120 mg/kg) and AR-A004 (110 mg/kg), respectively, compared to 50.18% for 5-fluorouracil (5-FU; 20 mg/kg). AR-A001 and AR-A004 were also significantly active in the leukemia model with 211.11% and 155.56% increase in mean survival time (MST) compared to a value of 211.11% for 5-FU. In conclusion, the ethanolic (AR-A001) and dichloromethane:methanol (AR-A004) root extracts of AR possess significant anticancer activities in vitro and in vivo.http://www.sciencedirect.com/science/article/pii/S2225411014000091Anticancer activityAristolochia ringensCytotoxicityLymphoid leukemiaSolid tumor
collection DOAJ
language English
format Article
sources DOAJ
author Abidemi James Akindele
Zahoor Wani
Girish Mahajan
Sadhana Sharma
Flora Ruth Aigbe
Naresh Satti
Olufunmilayo Olaide Adeyemi
Dilip Manikrao Mondhe
spellingShingle Abidemi James Akindele
Zahoor Wani
Girish Mahajan
Sadhana Sharma
Flora Ruth Aigbe
Naresh Satti
Olufunmilayo Olaide Adeyemi
Dilip Manikrao Mondhe
Anticancer activity of Aristolochia ringens Vahl. (Aristolochiaceae)
Journal of Traditional and Complementary Medicine
Anticancer activity
Aristolochia ringens
Cytotoxicity
Lymphoid leukemia
Solid tumor
author_facet Abidemi James Akindele
Zahoor Wani
Girish Mahajan
Sadhana Sharma
Flora Ruth Aigbe
Naresh Satti
Olufunmilayo Olaide Adeyemi
Dilip Manikrao Mondhe
author_sort Abidemi James Akindele
title Anticancer activity of Aristolochia ringens Vahl. (Aristolochiaceae)
title_short Anticancer activity of Aristolochia ringens Vahl. (Aristolochiaceae)
title_full Anticancer activity of Aristolochia ringens Vahl. (Aristolochiaceae)
title_fullStr Anticancer activity of Aristolochia ringens Vahl. (Aristolochiaceae)
title_full_unstemmed Anticancer activity of Aristolochia ringens Vahl. (Aristolochiaceae)
title_sort anticancer activity of aristolochia ringens vahl. (aristolochiaceae)
publisher Elsevier
series Journal of Traditional and Complementary Medicine
issn 2225-4110
publishDate 2015-01-01
description Cancer is a leading cause of death worldwide and sustained focus is on the discovery and development of newer and better tolerated anticancer drugs especially from plants. The sulforhodamine B (SRB) in vitro cytotoxicity assay, sarcoma-180 (S-180) ascites and solid tumor, and L1210 lymphoid leukemia in vivo models were used to investigate the anticancer activity of root extracts of Aristolochia ringens Vahl. (Aristolochiaceae; 馬兜鈴 mǎ dōu líng). AR-A001 (IC50 values of 20 μg/mL, 22 μg/mL, 3 μg/mL, and 24 μg/mL for A549, HCT-116, PC3, and THP-1 cell lines, respectively), and AR-A004 (IC50 values of 26 μg/mL, 19.5 μg/mL, 12 μg/mL, 28 μg/mL, 30 μg/mL, and 22 μg/mL for A549, HCT-116, PC3, A431, HeLa, and THP-1, respectively), were observed to be significantly active in vitro. Potency was highest with AR-A001 and AR-A004 for PC3 with IC50 values of 3 μg/mL and 12 μg/mL, respectively. AR-A001 and AR-A004 produced significant (p < 0.05–0.001) dose-dependent inhibition of tumor growth in the S-180 ascites model with peak effects produced at the highest dose of 120 mg/kg. Inhibition values were 79.51% and 89.98% for AR-A001 and AR-A004, respectively. In the S-180 solid tumor model, the inhibition of tumor growth was 29.45% and 50.50% for AR-A001 (120 mg/kg) and AR-A004 (110 mg/kg), respectively, compared to 50.18% for 5-fluorouracil (5-FU; 20 mg/kg). AR-A001 and AR-A004 were also significantly active in the leukemia model with 211.11% and 155.56% increase in mean survival time (MST) compared to a value of 211.11% for 5-FU. In conclusion, the ethanolic (AR-A001) and dichloromethane:methanol (AR-A004) root extracts of AR possess significant anticancer activities in vitro and in vivo.
topic Anticancer activity
Aristolochia ringens
Cytotoxicity
Lymphoid leukemia
Solid tumor
url http://www.sciencedirect.com/science/article/pii/S2225411014000091
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