Evidence map›Paper›PMID 35457226›Full record

ArticleInternational journal of molecular sciences2022

Synergistic Anti-Angiogenic Effect of Combined VEGFR Kinase Inhibitors, Lenvatinib, and Regorafenib: A Therapeutic Potential for Breast Cancer.

Khuloud Bajbouj, Rizwan Qaisar, Mohammed A Alshura, Zeinab Ibrahim, Mohamad B Alebaji, Amenah W Al Ani, Hanadi M Janajrah, Mariah M Bilalaga, Abdelrahman I Omara, Rebal S Abou Assaleh and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Khuloud BajboujCollege of Medicine, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.ORCID 0000-0001-7344-6095
Rizwan QaisarCollege of Medicine, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.
Mohammed A AlshuraCollege of Medicine, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.
Zeinab IbrahimCollege of Medicine, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.ORCID 0000-0002-0320-4127
Mohamad B AlebajiCollege of Medicine, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.ORCID 0000-0002-8114-0157
Amenah W Al AniCollege of Medicine, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.
Hanadi M JanajrahCollege of Medicine, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.
Mariah M BilalagaCollege of Medicine, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.
Abdelrahman I OmaraCollege of Medicine, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.
Rebal S Abou AssalehCollege of Medicine, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.
Maha M Saber-AyadCollege of Medicine, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.ORCID 0000-0002-9287-7621
Adel B ElmoselhiCollege of Medicine, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.ORCID 0000-0003-2152-6629
University of Sharjah · AE

Funding

University of Sharjah Project number 16010901012
6 · The paper itself

Abstract

Background: Breast cancer currently affects more than two million women worldwide, and its incidence is steadily increasing. One of the most essential factors of invasion and metastasis of breast cancer cells is angiogenesis and non-angiogenic vascularization. Lenvatinib and Regorafenib share the same anti-angiogenic effect by inhibiting vascular endothelial growth factor receptors (VEGFRs subtypes 1 to 3) and have been approved for treating different types of cancer. Methods: We investigated Lenvatinib and Regorafenib effects on a well-established in-vitro model of breast cancer using MCF-7 (estrogen, progesterone receptor-positive, and HER2-negative), MDA-MB-231 (triple negative), as well as Human Umbilical Vascular Endothelial Cell line (HUVEC) cell lines. We performed the cell viability assay on four groups of cells, which included a control group, a Lenvatinib treated only group, a Regorafenib treated only group, and a group treated with a combination of both drugs at 24, 48, and 72 h. Data were analyzed as means ± standard deviation, and the drug−drug interactions with Compusyn software. Cellular migration assay, tube formation assay, and Western blots were conducted to determine the functional and the protein expression of downstream signals such as Caspase-9, anti-apoptotic Survivin, P-ERK, and total-ERK in the control and treatment groups. Results: MCF-7 cells showed a reduction in cell survival rates with higher dosing and longer incubation periods with each drug and with the combination of drugs. A synergistic interaction was identified (CI < 1) with both drugs on MCF7 at different dose combinations and at a higher dose in MDA-MB-231 cells. Furthermore, there was a marked decrease in the anti-angiogenic effect of both drugs in tube formation assay using MDA-MB-231 cells and survivin protein expression in MCF-7, and those antitumor markers showed a better outcome in drug combination than the use of each drug alone. Conclusion: Our result is the first to report the synergistic anti-angiogenic potential of combination therapy of Lenvatinib and Regorafenib. Therefore, it shows their therapeutic potential in breast cancer, including the aggressive types. Further studies are warranted to confirm and explore this therapeutic approach.

Indexed as

Breast NeoplasmsAngiogenesis InhibitorsCell Line, TumorCell ProliferationFemaleHumansNeovascularization, PathologicPhenylurea CompoundsPyridinesQuinolinesSurvivinVascular Endothelial Growth Factor AAngiogenesis InhibitorslenvatinibPhenylurea CompoundsPyridinesQuinolinesregorafenibSurvivinVascular Endothelial Growth Factor Aangiogenesisbreast cancercancer therapychemotherapyLenvatinibRegorafenibVEGFR kinase inhibitors

Identifiers

PMID35457226
PMCPMC9028329
OpenAlexW4224008425

What Socratic 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 Socratic graph.