Evidence map›Paper›PMID 32153735›Full record

ArticleAvicenna journal of medical biotechnology

Expression of Human Placenta-specific 1 (PLAC1) in CHO-K1 Cells.

Jafar Mahmoudian, Mahboobeh Nazari, Roya Ghods, Mahmood Jeddi-Tehrani, Seyed Nasser Ostad, Mohammad Hossein Ghahremani, Sedigheh Vafaei, Mohammad Mehdi Amiri, Amir-Hassan Zarnani

Open access · greenAbstract read
In one paragraph

Article in Avicenna journal of medical biotechnology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

9 authors at 3 institutions in 1 country.

Jafar MahmoudianNanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences (TUMS), Tehran, Iran.
Mahboobeh NazariMonoclonal Antibody Research Center, Avicenna Research Institute (ACECR), Tehran, Iran.
Roya GhodsOncopathology Research Center, Iran University of Medical Sciences (IUMS), Tehran, Iran.
Mahmood Jeddi-TehraniMonoclonal Antibody Research Center, Avicenna Research Institute (ACECR), Tehran, Iran.
Seyed Nasser OstadNanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences (TUMS), Tehran, Iran.
Mohammad Hossein GhahremaniNanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences (TUMS), Tehran, Iran.
Sedigheh VafaeiReproductive Immunology Research Center, Avicenna Research Institute, (ACECR), Tehran, Iran.
Mohammad Mehdi AmiriDepartment of Immunology, School of Public Health, Tehran University of Medical Sciences (TUMS), Tehran, Iran.
Amir-Hassan ZarnaniReproductive Immunology Research Center, Avicenna Research Institute, (ACECR), Tehran, Iran.
Tehran University of Medical Sciences · IRAcademic Center for Education, Culture and Research · IRIran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPlacenta-specific 1 (PLAC1), as a new Cancer/Testis Antigen (CTA), is frequently expressed in a variety of cancers and localized to cytoplasm and plasma membrane. Surface expression of cancer target antigens is of great importance that enables antibody-mediated cancer immunotherapy. The aim of the current study was to express the intact human PLAC1 protein on plasma membrane of a eukaryotic cell as a model for future anti-PLAC1-based cancer immunotherapy.

methodsIn the first approach, entire human PLAC1 gene including its own Signal Peptide (SP) was cloned into pIRES2-EGFP and LeGO-iG2 vectors and expressed in CHO-K1 cells. In the second approach, cytosolic and Signal-Anchor (SA) sequence of Transferrin Receptor Protein 1 (TFR1) were fused to extracellular portion of PLAC1 and expressed as above. Expression of PLAC1 was then assessed using Reverse Transcription Polymerase Chain Reaction (RT-PCR), Western Blot (WB), Immunocytochemistry (ICC), Immunofluorescence (IF) and Flow Cytometry (FC).

resultsThe first approach resulted in the expression of PLAC1 in submembranous but not in the surface of transfected CHO-K1 cells. Using the chimeric human PLAC1 construct, the same intracellular expression pattern was observed.

conclusionThese results indicated that there are some yet unknown PLAC1 localization signals employed by cancer cells for surface expression of PLAC1.

Indexed as

Eukaryotic cellsPLAC1 protein expressionProtein transport

Identifiers

PMID32153735
PMCPMC7035464
OpenAlexW3013422543

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.