Evidence map›Paper›PMID 27824155›Full record

ArticleScientific reports2016

Cucurbitacin D exhibits potent anti-cancer activity in cervical cancer.

Mohammed Sikander, Bilal Bin Hafeez, Shabnam Malik, Abdulrhman Alsayari, Fathi T Halaweish, Murali M Yallapu, Subhash C Chauhan, Meena Jaggi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
6.0field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 78 citations in OpenAlex.

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  9. Modulatory Effect of Cucurbitacin D fromPharmaceuticals (Basel, Switzerland) · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Mohammed SikanderUniversity of Tennessee Health Science Centre, Memphis, TN, 38163, USA.
Bilal Bin HafeezUniversity of Tennessee Health Science Centre, Memphis, TN, 38163, USA.
Shabnam MalikUniversity of Tennessee Health Science Centre, Memphis, TN, 38163, USA.
Abdulrhman AlsayariKing Khaled University, College of Pharmacy, Box 188, Abha, 61441, Saudi Arabia.
Fathi T HalaweishSouth Dakota State University, Brookings, SD, 57007, USA.
Murali M YallapuUniversity of Tennessee Health Science Centre, Memphis, TN, 38163, USA.
Subhash C ChauhanUniversity of Tennessee Health Science Centre, Memphis, TN, 38163, USA.
Meena JaggiUniversity of Tennessee Health Science Centre, Memphis, TN, 38163, USA.
University of Tennessee Health Science Center · USKing Khaled Hospital · SASouth Dakota State University · US

Funding

Etiology of cervical cancer health disparity in American Indian womenU01CA162106 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CHAUHAN, SUBHASH C., JAGGI, MEENA · 2012 to 2016
$1.5M
Aspects of MUC13 Mucin in CancerR01CA142736 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CHAUHAN, SUBHASH C. · 2010 to 2013
$1.2M
PSMA Targeted Docetaxel Loaded Magnetic Nanoparticles for Prostate Cancer TherapyK22CA174841 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI YALLAPU, MURALI MOHAN · 2015 to 2017
$485k
NCI NIH HHS K22 CA174841NCI NIH HHS R01 CA142736NCI NIH HHS U01 CA162106
6 · The paper itself

Abstract

In this study, we for the first time, investigated the potential anti-cancer effects of a novel analogue of cucurbitacin (Cucurbitacin D) against cervical cancer in vitro and in vivo. Cucurbitacin D inhibited viability and growth of cervical cancer cells (CaSki and SiHa) in a dose-dependent manner. IC50 of Cucurbitacin D was recorded at 400 nM and 250 nM in CaSki and SiHa cells, respectively. Induction of apoptosis was observed in Cucurbitacin D treated cervical cancer cells as measured by enhanced Annexin V staining and cleavage in PARP protein. Cucurbitacin D treatment of cervical cancer cells arrested the cell cycle in G1/S phase, inhibited constitutive expression of E6, Cyclin D1, CDK4, pRb, and Rb and induced the protein levels of p21 and p27. Cucurbitacin D also inhibited phosphorylation of STAT3 at Ser727 and Tyr705 residues as well as its downstream target genes c-Myc, and MMP9. Cucurbitacin D enhanced the expression of tumor suppressor microRNAs (miR-145, miRNA-143, and miRNA34a) in cervical cancer cells. Cucurbitacin D treatment (1 mg/kg body weight) effectively inhibited growth of cervical cancer cells derived orthotopic xenograft tumors in athymic nude mice. These results demonstrate the potential therapeutic efficacy of Cucurbitacin D against cervical cancer.

Indexed as

AnimalsApoptosisCell Line, TumorFemaleG1 Phase Cell Cycle CheckpointsGene Expression Regulation, NeoplasticHumansMice, NudeNeoplasm ProteinsS Phase Cell Cycle CheckpointsTriterpenesUterine Cervical NeoplasmsXenograft Model Antitumor Assayscucurbitacin DNeoplasm ProteinsTriterpenes

Identifiers

PMID27824155
PMCPMC5100479
OpenAlexW2555729922

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.