Fractionated Leaf Extracts of Ocimum gratissimum Inhibit the Proliferation and Induce Apoptosis of A549 Lung Adenocarcinoma Cells

Author:

Curtis Rachael M.1,Wang Heng-Shan2,Luo Xuan3,Dugo Erika B.4,Stevens Jacqueline J.1,Tchounwou Paul B.15ORCID

Affiliation:

1. College of Science, Engineering, and Technology, Jackson State University, 1400 JR Lynch Street, Jackson, MS 39217, USA

2. School of Chemistry and Pharmacy, Guangxi Normal University, No. 15 Yu Cai Road, Guilin 541004, China

3. Department of Applied Chemistry, School of Chemistry and Chemical Engineering, Guangxi University, No. 100 East Daxue Road, Nanning 530004, China

4. Department of Natural and Behavioral Sciences, College of Science, Technology, Engineering, and Mathematics, Johnson C. Smith University, 100 Beatties Ford Road, Charlotte, NC 28216, USA

5. RCMI Center for Urban Health Disparities Research and Innovation, Morgan State University, 1700 E. Cold Spring Lane, Baltimore, MD 21252, USA

Abstract

Previous in vitro studies in our laboratory demonstrated that ethyl acetate (P2) and water- soluble (PS/PT1) fractionated leaf extracts of Ocimum gratissimum inhibit the proliferation of prostate cancer cells. It has been reported that the crude aqueous extract induces apoptosis in lung adenocarcinoma cells; however, the efficacy of the fractionated extracts against these cells remains unclear. In the present study, we hypothesized that the ability of the fractionated extracts to inhibit proliferation and induce apoptosis is associated with the activation of pro-apoptotic proteins and induction of DNA condensation in A549 cells. Ocimum gratissimum was cultivated and its leaves were harvested, extracted, and fractionated to produce fractions P2 and PS/PT1. Anti-proliferative activity was assessed by direct cell count. For morphological characterization of apoptosis, 4′,6-diamidino-2-phenylindole staining was employed. Western blot analysis was performed to evaluate the apoptotic activity of the fractionated extracts. In data generated from anti-proliferation studies, P2 significantly inhibited cell proliferation in a concentration-dependent manner; PS/PT1 elicited a decrease in the viability of cells, occurring at 500 µg/mL. 4′,6-diamidino-2-phenylindole staining revealed the induction of apoptosis, as evidenced by the formation of apoptotic bodies. Increased levels of pro-apoptotic proteins were observed as the concentrations of the fractionated extracts increased. These results suggest that fractionated leaf extracts of Ocimum gratissimum inhibit the proliferation and induce apoptosis of A549 cells.

Funder

RCMI Center for Health Disparities Research and Innovation at Morgan State University, Baltimore, Maryland, USA

Research Initiative for Scientific Enhancement (RISE) Program at Jackson State University, Jackson, Mississippi, USA

Scientific Research Foundation of Guangxi University, Guangxi, China

National Institutes of Health

Publisher

MDPI AG

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