Evidence map›Paper›PMID 35269621›Full record

ArticleInternational journal of molecular sciences2022

Biological Effects of Cyclin-Dependent Kinase Inhibitors Ribociclib, Palbociclib and Abemaciclib on Breast Cancer Bone Microenvironment.

Michele Iuliani, Sonia Simonetti, Giulia Ribelli, Andrea Napolitano, Umile Giuseppe Longo, Bruno Vincenzi, Paolo Orsaria, Vincenzo Denaro, Giuseppe Tonini, Daniele Santini and 1 more

Open 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. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

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  9. Cancer treatment-induced bone loss.The Korean journal of internal medicine · 2024
    Review
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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

11 authors at 1 institution in 2 countries.

Michele IulianiDepartment of Medical Oncology, Campus Bio-Medico University of Rome, 00128 Rome, Italy.ORCID 0000-0003-3536-7630
Sonia SimonettiDepartment of Medical Oncology, Campus Bio-Medico University of Rome, 00128 Rome, Italy.
Giulia RibelliDepartment of Medical Oncology, Campus Bio-Medico University of Rome, 00128 Rome, Italy.
Andrea NapolitanoDepartment of Medical Oncology, Campus Bio-Medico University of Rome, 00128 Rome, Italy.ORCID 0000-0002-7509-1555
Umile Giuseppe LongoDepartment of Orthopedic and Trauma Surgery, Campus Bio-Medico University of Rome, 00128 Rome, Italy.
Bruno VincenziDepartment of Medical Oncology, Campus Bio-Medico University of Rome, 00128 Rome, Italy.
Paolo OrsariaDepartment of Breast Surgery, Campus Bio-Medico University Hospital of Rome, 00128 Rome, Italy.
Vincenzo DenaroDepartment of Orthopedic and Trauma Surgery, Campus Bio-Medico University of Rome, 00128 Rome, Italy.
Giuseppe ToniniDepartment of Medical Oncology, Campus Bio-Medico University of Rome, 00128 Rome, Italy.
Daniele SantiniDepartment of Medical Oncology, Campus Bio-Medico University of Rome, 00128 Rome, Italy.
Pantano FrancescoDepartment of Medical Oncology, Campus Bio-Medico University of Rome, 00128 Rome, Italy.
Università Campus Bio-Medico · IT

Funding

Novartis (Italy) NA
6 · The paper itself

Abstract

The CDK4/6 inhibitors (CDKi) palbociclib, ribociclib, and abemaciclib are currently approved in combination with anti-estrogen therapy for the treatment of advanced and/or metastatic hormone receptor-positive/HER2-neu-negative breast cancer patients. Given the high incidence of bone metastases in this population, we investigated and compared the potential effects of palbociclib, ribociclib, and abemaciclib on the breast cancer bone microenvironment. Primary osteoclasts (OCs) and osteoblasts (OBs) were obtained from human monocyte and mesenchymal stem cells, respectively. OC function was evaluated by tartrate-resistant acid phosphatase assay and real-time PCR; OB activity was assessed by an alizarin red assay. OB/breast cancer co-culture models were generated via the seeding of MCF-7 cells on a layer of OBs, and tumor cell proliferation was analyzed using flow cytometry. Here, we showed that ribociclib, palbociclib, and abemaciclib exerted similar inhibitory effects on the OC differentiation and expression of bone resorption markers without affecting OC viability. On the other hand, the three CDKi did not affect the ability of OB to produce bone matrix, even if the higher doses of palbociclib and abemaciclib reduced the OB viability. In OB/MCF-7 co-culture models, palbociclib demonstrated a lower anti-tumor effect than ribociclib and abemaciclib. Overall, our results revealed the direct effects of CDKi on the tumor bone microenvironment, highlighting differences potentially relevant for clinical practice.

Indexed as

Breast NeoplasmsAminopyridinesBenzimidazolesCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Cyclin-Dependent Kinase Inhibitor ProteinsFemaleHumansPiperazinesProtein Kinase InhibitorsPurinesPyridinesTumor MicroenvironmentabemaciclibAminopyridinesBenzimidazolesCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Cyclin-Dependent Kinase Inhibitor ProteinspalbociclibPiperazinesProtein Kinase InhibitorsPurinesPyridinesribociclibbone tumor microenvironmentbreast cancerCDK4/6 inhibitorsosteoblastsosteoclasts

Identifiers

PMID35269621
PMCPMC8910497
OpenAlexW4213416537

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.