Downregulation of Stemness Genes and Induction of Necrosis in Rat LA7 Cancer Stem Cells Induced Tumors Treated with Starved Fibroblasts Culture Supernatant.

Breast cancer Cancer Stem cells Cell differentiation Fibroblasts Gene expression

Journal

Reports of biochemistry & molecular biology
ISSN: 2322-3480
Titre abrégé: Rep Biochem Mol Biol
Pays: Iran
ID NLM: 101637937

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 28 09 2020
accepted: 11 10 2020
entrez: 19 7 2021
pubmed: 20 7 2021
medline: 20 7 2021
Statut: ppublish

Résumé

Stem cell differentiation therapy is a promising strategy in cancer treatment. we show that protein cocktail prepared from serum starved fibroblasts has therapeutic potential based on this strategy. The condition medium was prepared from foreskin isolated fibroblasts and analyzed by Liquid chromatography electrospray ionization mass spectrometry-mass spectrometry (LC-ESI-MS/MS). LA7 mammary gland cancer stem cells originated tumors were induced in Sprague Dawley rats. The rats treated subcutaneously with DMEM (group A), condition medium (group B), or normal saline (group C) once daily for 7 days. Then the tumors were removed and divided into the two parts, one part was used to quantify gene expression by stem-loop RT-qPCR assay and the other part was used for Hematoxylin & Eosin (H & E), Giemsa, and immunohistochemistry (IHC) staining. All induced tumors appeared as sarcomatoid carcinoma (SC). Immunohistochemistry staining confirmed this conclusion by recognizing the tumor as Ki67 This study showed that the substances released from starved human fibroblasts were able to down-regulate the stemness-related genes and induce necrosis in LA7 derived tumors.

Sections du résumé

BACKGROUND BACKGROUND
Stem cell differentiation therapy is a promising strategy in cancer treatment. we show that protein cocktail prepared from serum starved fibroblasts has therapeutic potential based on this strategy.
METHODS METHODS
The condition medium was prepared from foreskin isolated fibroblasts and analyzed by Liquid chromatography electrospray ionization mass spectrometry-mass spectrometry (LC-ESI-MS/MS). LA7 mammary gland cancer stem cells originated tumors were induced in Sprague Dawley rats. The rats treated subcutaneously with DMEM (group A), condition medium (group B), or normal saline (group C) once daily for 7 days. Then the tumors were removed and divided into the two parts, one part was used to quantify gene expression by stem-loop RT-qPCR assay and the other part was used for Hematoxylin & Eosin (H & E), Giemsa, and immunohistochemistry (IHC) staining.
RESULTS RESULTS
All induced tumors appeared as sarcomatoid carcinoma (SC). Immunohistochemistry staining confirmed this conclusion by recognizing the tumor as Ki67
CONCLUSION CONCLUSIONS
This study showed that the substances released from starved human fibroblasts were able to down-regulate the stemness-related genes and induce necrosis in LA7 derived tumors.

Identifiants

pubmed: 34277874
doi: 10.52547/rbmb.10.1.105
pii: rbmb-10-105
pmc: PMC8279721
doi:

Types de publication

Journal Article

Langues

eng

Pagination

105-118

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Auteurs

Roghayeh Pourbagher (R)

Student Research Committee, Babol University of Medical Sciences, Babol, Iran.
Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.

Hossein Ghorbani (H)

Department of Pathology, Rohani Hospital, Babol University of Medical Sciences, Babol, Iran.

Haleh Akhavan-Niaki (H)

Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.

Seyed Gholam Ali Jorsaraei (SGA)

Fatemeh Zahra Infertility and Reproductive Health Research Centre, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.

Sadegh Fattahi (S)

Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.

Sahar Ghooran (S)

Department of Pathology, Rohani Hospital, Babol University of Medical Sciences, Babol, Iran.

Zeinab Abedian (Z)

Student Research Committee, Babol University of Medical Sciences, Babol, Iran.
Dental Materials Research Center, Dental Faculty, Babol University of Medical Sciences, Babol, Iran.

Masoumeh Ghasemi (M)

Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.

Fatemeh Saeedi (F)

Student Research Committee, Babol University of Medical Sciences, Babol, Iran.
Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.

Negar Jafari (N)

Student Research Committee, Babol University of Medical Sciences, Babol, Iran.
Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.

Behnam Kalali (B)

Institute for Medical Microbiology, Immunology and Hygiene, Technische Universität München, Munich, Germany.

Amrollah Mostafazadeh (A)

Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.

Classifications MeSH