Evidence map›Paper›PMID 36614128›Full record

ArticleInternational journal of molecular sciences2022

Active Targeting of Versatile Nanocomplex Using the Novel Biomarker of Breast Cancer Stem Cells.

Eun-Young Koh, Keun-Sik Kim, Hee-Bin Park, Jong-Seok Kim, Pyung-Hwan Kim

Abstract 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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Advanced drug delivery platforms target cancer stem cells.Asian journal of pharmaceutical sciences · 2025
    Review
  3. Article
  4. Review
  5. 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

5 authors.

Eun-Young KohDepartment of Biomedical Laboratory Science, Konyang University, Daejeon 35365, Republic of Korea.ORCID 0000-0002-3119-3285
Keun-Sik KimDepartment of Biomedical Laboratory Science, Konyang University, Daejeon 35365, Republic of Korea.
Hee-Bin ParkDepartment of Biomedical Laboratory Science, Konyang University, Daejeon 35365, Republic of Korea.
Jong-Seok KimMyunggok Medical Research Institute, College of Medicine, Konyang University, Daejeon 35365, Republic of Korea.ORCID 0000-0002-0998-5569
Pyung-Hwan KimDepartment of Biomedical Laboratory Science, Konyang University, Daejeon 35365, Republic of Korea.ORCID 0000-0002-3117-4025

Funding

Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education 2020R1F1A1053663
6 · The paper itself

Abstract

Breast cancer in women is one of the most common life-threatening malignancies. Despite of the development for the improved treatment, there are still many limitations to overcome. Among them, cancer stem cells (CSCs) are well known for tumor formation, development, cellular heterogeneity, and cancer recurrence. Therefore, to completely cure breast cancer, treatment of both cancer and CSC is required. To selectively target CSCs, we generated a liposome-based smart nano complex using CEACAM 6 (CD66c) antibody (Ab), a novel cell-surface biomarker of breast-derived CSCs (BCSCs) discovered in our previous research. Selective and increased cellular uptake was observed in BCSCs treated with CD66c Ab-conjugated rhodamine-labeled liposomes (CDRHOL) depending on the expression level of CD66c. CD66c Ab-conjugated doxorubicin (DOX)-loaded liposomes (CDDOXL) selectively showed increased cell killing effects in BCSCs with high CD66c expression levels. In an in vivo animal study, CDRHOL showed enhanced accumulation in xenografted BCSC tumors with low delivery into non-target organs. Moreover, mice treated with CDDOXL have assessed the decreased induction ability of immune response by low expression levels of pro-inflammatory cytokines and reduced liver toxicity by histopathological analysis. Finally, the improved antitumor effect of CDDOXL was evaluated in a metastatic BCSC mouse model via systemic administration. Collectively, our study is the first to demonstrate that a multi-functional nano complex using a novel surface biomarker of BCSC may be a more effective therapeutic agent for the treatment of cancer and CSCs.

Indexed as

LiposomesNeoplasm Recurrence, LocalAnimalsBiomarkersCell Line, TumorDoxorubicinFemaleMiceNeoplastic Stem CellsPolyethylene GlycolsBiomarkersDoxorubicinliposomal doxorubicinLiposomesPolyethylene Glycolsactive targetingbreast cancer stem cellCD66csurface biomarkertherapeutic nanocomplex

Identifiers

PMID36614128
PMCPMC9821020

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.