Literature DB >> 33006711

Osteopontin-4 and Osteopontin-5 splice variants are expressed in several tumor cell lines.

Gabriela Ribeiro Silva1,2, Daniella Santos Mattos1,3, Ana Clara Fonseca Bastos1,3, Bruna Prunes Pena Baroni Viana1,3, Mariana Concentino Menezes Brum1,3, Luciana Bueno Ferreira1,3, Etel Rodrigues Pereira Gimba4,5,6,7,8.   

Abstract

Among osteopontin splice variants (OPN-SV), the expression profile of osteopontin-4 (OPN4) and osteopontin-5 (OPN5) has not been addressed in distinct cancer types. We herein aimed to investigate their expression in several cancer cell lines, besides comparing it in relation to the three previously described OPN-SV: OPNa, OPNb and OPNc. Total RNA from cancer cell lines, including prostate (PC3 and DU145), ovarian (A2780), breast (MCF-7 and MDA-MB-231), colorectal (Caco-2, HT-29 and HCT-116), thyroid (TT, TPC1 and 8505c) and lung (A549 and NCI-H460) was extracted, followed by cDNA synthesis. OPN-SV transcript analysis by RT-PCR or RT-qPCR were performed using OPN-SV specific oligonucleotides and gapdh and actin transcripts were used as housekeeping controls. OPN4 and OPN5 transcripts displayed co-expression in most tested cell lines. OPN4 was found expressed in similar or higher levels in relation to OPN5. Moreover, in most tested cell lines, OPN4 is also expressed in similar levels to OPNa or OPNb. The expression of OPN5 is also generally variable in relation to the other OPN-SV, but expressed in similar or higher levels in relation to OPNc, depending on each tested cell line. OPN4 and OPN5 seem to be co-expressed in several tumor types and OPN4 is one of the most overexpressed OPN-SV in distinct tumor cell lines. Once both OPN4 and OPN5 are differentially expressed and also evidence tumor-specific expression patterns, we hypothesize that similarly to the other OPN-SV, they also possibly contribute to key aspects of tumor progression, what should be further functionally investigated in distinct tumor models.

Entities:  

Keywords:  Cancer cell lines; OPN4; OPN5; Osteopontin; Splice variants; Splicing

Mesh:

Substances:

Year:  2020        PMID: 33006711     DOI: 10.1007/s11033-020-05867-9

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  4 in total

1.  CRISPR/Cas9 mediated knocking out of OPN gene enhances radiosensitivity in MDA-MB-231 breast cancer cell line.

Authors:  Rahil Ghanbarnasab Behbahani; Amir Danyaei; Ali Teimoori; Mohammad Javad Tahmasbi; Niloofar Neisi
Journal:  J Cancer Res Clin Oncol       Date:  2022-08-30       Impact factor: 4.322

Review 2.  The Role of Osteopontin in Tumor Progression Through Tumor-Associated Macrophages.

Authors:  Yuying Tan; Lei Zhao; Yong-Guang Yang; Wentao Liu
Journal:  Front Oncol       Date:  2022-07-08       Impact factor: 5.738

3.  Gene Expression Patterns of Osteopontin Isoforms and Integrins in Malignant Melanoma.

Authors:  Krisztina Jámbor; Viktória Koroknai; Tímea Kiss; István Szász; Péter Pikó; Margit Balázs
Journal:  Pathol Oncol Res       Date:  2022-08-24       Impact factor: 2.874

4.  Expression of osteopontin-5 splice variant in the mouse primary and metastatic breast cancer cells.

Authors:  Mohammad Kamalabadi-Farahani; Amir Atashi; Zahra Jabbarpour; Seyed Sajjad Aghayan
Journal:  BMC Res Notes       Date:  2022-09-05
  4 in total

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