Evidence map›Paper›PMID 30546830›Full record

ArticleOncotarget2018

Inhibition of breast cancer metastasis to the lungs with UBS109.

Mamoru Shoji, Wei Ping Qian, Ganji Purnachandra Nagaraju, Daniel J Brat, Danielle Pessolano, Rick Luzietti, Spandan Chennamadhavuni, Masayoshi Yamaguchi, Lily Yang, Dennis C Liotta

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 18% 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

3 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

10 authors at 3 institutions in 1 country.

Mamoru ShojiDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA.
Wei Ping QianDepartment of Surgery, Emory University, Atlanta, GA 30322, USA.
Ganji Purnachandra NagarajuDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA.
Daniel J BratDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA.
Danielle PessolanoAgilux Laboratories, Inc./Charles River Laboratories, Inc., Worcester, MA 01608, USA.
Rick LuziettiAgilux Laboratories, Inc./Charles River Laboratories, Inc., Worcester, MA 01608, USA.
Spandan ChennamadhavuniEmory Institute for Drug Development, Emory University, Atlanta, GA 30322, USA.
Masayoshi YamaguchiDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA.
Lily YangDepartment of Surgery, Emory University, Atlanta, GA 30322, USA.
Dennis C LiottaEmory Institute for Drug Development, Emory University, Atlanta, GA 30322, USA.
Emory University · USCharles River Laboratories (United States) · USNorthwestern Medicine · US

Funding

Targeted Therapy of Triple Negative Breast Cancer Using Theranostic NanoparticlesR01CA154129 · NCI · EMORY UNIVERSITY · PI YANG, LILY · 2011 to 2015
$1.7M
Targeted Delivery of a Novel Synthetic Curcumin Analog, EF24 to Glioblastoma andR21CA139035 · NCI · EMORY UNIVERSITY · PI BRAT, DANIEL J, SHOJI, MAMORU NONE · 2011 to 2012
$371k
NCI NIH HHS R01 CA154129NCI NIH HHS R21 CA139035
6 · The paper itself

Abstract

Synthetic monocarbonyl analogs of curcumin (MACs) are cytotoxic against several cancers including head and neck cancer, pancreatic cancer, colon cancer, and breast cancer. Mechanisms of action include depolarization of the mitochondrial membrane potential and inhibition of NF-κB, leading to apoptosis. We previously demonstrated that UBS109 (MAC), has preventive effects on bone loss induced by breast cancer cell lines. We determined whether UBS109 could inhibit and prevent lung metastasis, since lung metastasis of breast cancer is a major problem in addition to bone metastasis. A breast cancer lung metastasis (colonization) model was created by injection of breast cancer cells MDA-MB-231 into the tail vein of athymic nude mice, nu/nu. Animals were treated with vehicle or UBS109 at 5 or 15 mg/kg body weight by intraperitoneal injection once daily 5 days a week for 5 weeks. UBS109 at 15 mg/kg significantly inhibited lung metastasis/colonization as demonstrated by reduced lung weight consisting of tumor nodules. The body weight of animals treated with UBS109 15 mg/kg remained the same as in the other groups. UBS109 killed completely (100%) MDA-MB-231 breast cancer cells at 1.25 μM in a cytotoxicity assay

Indexed as

bone metastasisbreast cancerlung metastasesMACsUBS109

Identifiers

PMID30546830
PMCPMC6281413
OpenAlexW2901690551

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.