scholarly journals Bioprospecting of Natural Compounds from Brazilian Cerrado Biome Plants in Human Cervical Cancer Cell Lines

2021 ◽  
Vol 22 (7) ◽  
pp. 3383
Author(s):  
Marcela N. Rosa ◽  
Larissa R. V. e Silva ◽  
Giovanna B. Longato ◽  
Adriane F. Evangelista ◽  
Izabela N. F. Gomes ◽  
...  

Cervical cancer is the third most common in Brazilian women. The chemotherapy used for the treatment of this disease can cause many side effects; then, to overcome this problem, new treatment options are necessary. Natural compounds represent one of the most promising sources for the development of new drugs. In this study, 13 different species of 6 families from the Brazilian Cerrado vegetation biome were screened against human cervical cancer cell lines (CCC). Some of these species were also evaluated in one normal keratinocyte cell line (HaCaT). The effect of crude extracts on cell viability was evaluated by a colorimetric method (MTS assay). Extracts from Annona crassiflora, Miconia albicans, Miconia chamissois, Stryphnodendron adstringens, Tapirira guianensis, Xylopia aromatica, and Achyrocline alata showed half-maximal inhibitory concentration (IC50) values < 30 μg/mL for at least one CCC. A. crassiflora and S. adstringens extracts were selective for CCC. Mass spectrometry (Electrospray Ionization Fourier Transform Ion Cyclotron Resonance Mass Spectrometer (ESI FT-ICR MS)) of A. crassiflora identified fatty acids and flavonols as secondary compounds. One of the A. crassiflora fractions, 7C24 (from chloroform partition), increased H2AX phosphorylation (suggesting DNA damage), PARP cleavage, and cell cycle arrest in CCC. Kaempferol-3-O-rhamnoside and oleic acid were bioactive molecules identified in 7C24 fraction. These findings emphasize the importance of investigating bioactive molecules from natural sources for developing new anti-cancer drugs.

2008 ◽  
Vol 127 ◽  
pp. S147
Author(s):  
Luis Jave-Suarez ◽  
Naela Arreygue-Garcia ◽  
Adriana Aguilar-Lemarrroy ◽  
Miriam Jimenez-Perez ◽  
Angel Arregui ◽  
...  

2018 ◽  
Vol 37 (4) ◽  
pp. 602-615 ◽  
Author(s):  
Viviane A. O. Silva ◽  
Ana Laura V. Alves ◽  
Marcela N. Rosa ◽  
Larissa R. V. Silva ◽  
Matias E. Melendez ◽  
...  

2014 ◽  
Vol 92 (2) ◽  
pp. 95-104 ◽  
Author(s):  
Aline Beckenkamp ◽  
Danielle Bertodo Santana ◽  
Alessandra Nejar Bruno ◽  
Luciane Noal Calil ◽  
Emerson André Casali ◽  
...  

Cervical cancer is the third most frequent cancer in women worldwide. Adenine nucleotide signaling is modulated by the ectonucleotidases that act in sequence, forming an enzymatic cascade. Considering the relationship between the purinergic signaling and cancer, we studied the E-NTPDases, ecto-5′-nucleotidase, and E-NPPs in human cervical cancer cell lines and keratinocytes. We evaluated the expression profiles of these enzymes using RT-PCR and quantitative real-time PCR analysis. The activities of these enzymes were examined using ATP, ADP, AMP, and p-nitrophenyl-5′-thymidine monophosphate (p-Nph-5′-TMP) as substrate, in a colorimetric assay. The extracellular adenine nucleotide hydrolysis was estimated by HPLC analysis. The hydrolysis of all substrates exhibited a linear pattern and these activities were cation-dependent. An interesting difference in the degradation rate was observed between cervical cancer cell lines SiHa, HeLa, and C33A and normal imortalized keratinocytes, HaCaT cells. The mRNA of ecto-5′-nucleotidase, E-NTPDases 5 and 6 were detectable in all cell lines, and the dominant gene expressed was the Entpd 5 enzyme, in SiHa cell line (HPV16 positive). In accordance with this result, a higher hydrolysis activity for UDP and GDP nucleotides was observed in the supernatant of the SiHa cells. Both normal and cancer cells presented activity and mRNAs of members of the NPP family. Considering that these enzymes exert an important catalytic activity, controlling purinergic nucleotide concentrations in tumors, the presence of ectonucleotidases in cervical cancer cells can be important to regulate the levels of extracellular adenine nucleotides, limiting their effects.


2006 ◽  
Vol 12 (1) ◽  
pp. 250-256 ◽  
Author(s):  
Christopher M. Lee ◽  
Christa B. Fuhrman ◽  
Vicente Planelles ◽  
Morgan R. Peltier ◽  
David K. Gaffney ◽  
...  

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