» Articles » PMID: 35745070

Screening of Specific and Common Pathways in Breast Cancer Cell Lines MCF-7 and MDA-MB-231 Treated with Chlorophyllides Composites

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2022 Jun 24
PMID 35745070
Authors
Affiliations
Soon will be listed here.
Abstract

Our previous findings have shown that the chlorophyllides composites have anticancer activities to breast cancer cell lines (MCF-7 and MDA-MB-231). In the present study, microarray gene expression profiling was utilized to investigate the chlorophyllides anticancer mechanism on the breast cancer cells lines. Results showed that chlorophyllides composites induced upregulation of 43 and 56 differentially expressed genes (DEG) in MCF-7 and MDA-MB-231 cells, respectively. In both cell lines, chlorophyllides composites modulated the expression of annexin A4 (ANXA4), chemokine C-C motif receptor 1 (CCR1), stromal interaction molecule 2 (STIM2), ethanolamine kinase 1 (ETNK1) and member of RAS oncogene family (RAP2B). Further, the KEGG annotation revealed that chlorophyllides composites modulated DEGs that are associated with the endocrine system in MCF-7 cells and with the nervous system in MDA-MB-231 cells, respectively. The expression levels of 9 genes were validated by quantitative reverse transcription PCR (RT-qPCR). The expression of CCR1, STIM2, ETNK1, MAGl1 and TOP2A were upregulated in both chlorophyllides composites treated-MCF-7 and MDA-MB-231 cells. The different expression of NLRC5, SLC7A7 and PKN1 provided valuable information for future investigation and development of novel cancer therapy.

Citing Articles

Synergistic Anticancer Efficacy of Curcumin and Doxorubicin Combination Treatment Inducing S-phase Cell Cycle Arrest in Triple-Negative Breast Cancer Cells: An In Vitro Study.

Sarkar E, Khan A, Ahmad R, Misra A, Raza S, Mahdi A Cureus. 2025; 16(12):e75047.

PMID: 39749050 PMC: 11695051. DOI: 10.7759/cureus.75047.


BET inhibitor and CDK4/6 inhibitor synergistically inhibit breast cancer by suppressing BRD4 stability and DNA damage repair.

Chi S, Wei F, Li Y, Yu L, Ma C, Fang Y Transl Oncol. 2024; 51:102212.

PMID: 39591896 PMC: 11629338. DOI: 10.1016/j.tranon.2024.102212.


Perilla-Leaf-Derived Extracellular Vesicles Selectively Inhibit Breast Cancer Cell Proliferation and Invasion.

Kim D, Kang S, Rhee W Int J Mol Sci. 2023; 24(21).

PMID: 37958616 PMC: 10647566. DOI: 10.3390/ijms242115633.


Isogenic Cell Lines Derived from Specific Organ Metastases Exhibit Divergent Cytogenomic Aberrations.

Winnard Jr P, Morsberger L, Yonescu R, Jiang L, Zou Y, Raman V Cancers (Basel). 2023; 15(5).

PMID: 36900209 PMC: 10000985. DOI: 10.3390/cancers15051420.

References
1.
Akram I, Georges R, Hielscher T, Adwan H, Berger M . The chemokines CCR1 and CCRL2 have a role in colorectal cancer liver metastasis. Tumour Biol. 2015; 37(2):2461-71. DOI: 10.1007/s13277-015-4089-4. View

2.
Hortobagyi G . Treatment of breast cancer. N Engl J Med. 1998; 339(14):974-84. DOI: 10.1056/NEJM199810013391407. View

3.
Reis-Filho J, Pusztai L . Gene expression profiling in breast cancer: classification, prognostication, and prediction. Lancet. 2011; 378(9805):1812-23. DOI: 10.1016/S0140-6736(11)61539-0. View

4.
Ezzati M, Yousefi B, Velaei K, Safa A . A review on anti-cancer properties of Quercetin in breast cancer. Life Sci. 2020; 248:117463. DOI: 10.1016/j.lfs.2020.117463. View

5.
Chou Y, Ko C, Yen C, Chen L, Shaw J . A Novel Recombinant Chlorophyllase1 from Chlamydomonas reinhardtii for the Production of Chlorophyllide Derivatives. J Agric Food Chem. 2015; 63(43):9496-503. DOI: 10.1021/acs.jafc.5b02787. View