Evidence map›Paper›PMID 31165204›Full record

ReviewCancer immunology, immunotherapy : CII2019

PLAC1: biology and potential application in cancer immunotherapy.

Jafar Mahmoudian, Roya Ghods, Mahboobeh Nazari, Mahmood Jeddi-Tehrani, Mohammad Hossein Ghahremani, Nassim Ghaffari-Tabrizi-Wizsy, Seyed Nasser Ostad, Amir-Hassan Zarnani

Open access · greenAbstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  6. Placenta: an old organ with new functions.Frontiers in immunology · 2024
    Review
  7. Article
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  10. Review
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  14. Placenta-specific protein 1 enhances liver metastatic potential and is associated with the PI3K/AKT/NF-κB signaling pathway in colorectal cancer.European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) · 2021
    Article
  15. Article
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  18. 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

8 authors at 4 institutions in 2 countries.

Jafar MahmoudianNanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences (TUMS), Tehran, Iran.
Roya GhodsOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Mahboobeh NazariMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Mahmood Jeddi-TehraniMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Mohammad Hossein GhahremaniNanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences (TUMS), Tehran, Iran.
Nassim Ghaffari-Tabrizi-WizsySFL Chicken CAM Lab, Institute of Pathophysiology and Immunology, Medical University of Graz, 8010, Graz, Austria.
Seyed Nasser OstadNanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences (TUMS), Tehran, Iran. ostadnas@tums.ac.ir.
Amir-Hassan ZarnaniDepartment of Immunology, School of Public Health, Tehran University of Medical Sciences, Nafisi Building, Enghelab St., Tehran, 1417613151, Iran. zarnania@tums.ac.ir.
Academic Center for Education, Culture and Research · IRTehran University of Medical Sciences · IRIran University of Medical Sciences · IRMedical University of Graz · AT

Funding

Avicenna Research Institute 960511-036Tehran University of Medical Sciences 94-01-57-27939
6 · The paper itself

Abstract

The emergence of immunotherapy has revolutionized medical oncology with unprecedented advances in cancer treatment over the past two decades. However, a major obstacle in cancer immunotherapy is identifying appropriate tumor-specific antigens to make targeted therapy achievable with fewer normal cells being impaired. The similarity between placentation and tumor development and growth has inspired many investigators to discover antigens for effective immunotherapy of cancers. Placenta-specific 1 (PLAC1) is one of the recently discovered placental antigens with limited normal tissue expression and fundamental roles in placental function and development. There is a growing body of evidence showing that PLAC1 is frequently activated in a wide variety of cancer types and promotes cancer progression. Based on the restricted expression of PLAC1 in testis, placenta and a wide variety of cancers, we have designated this molecule with new terminology, cancer-testis-placenta (CTP) antigen, a feature that PLAC1 shares with many other cancer testis antigens. Recent reports from our lab provide compelling evidence on the preferential expression of PLAC1 in prostate cancer and its potential utility in prostate cancer immunotherapy. PLAC1 may be regarded as a potential CTP antigen for targeted cancer immunotherapy based on the available data on its promoting function in cancer development and also its expression in cancers of different histological origin. In this review, we will summarize current data on PLAC1 with emphasis on its association with cancer development and immunotherapy.

Indexed as

Antigens, NeoplasmAntineoplastic Agents, ImmunologicalBiomarkers, TumorDisease ProgressionFemaleHumansImmunotherapyMaleMolecular Targeted TherapyNeoplasmsPlacentaPregnancyPregnancy ProteinsTestisAntigens, NeoplasmAntineoplastic Agents, ImmunologicalBiomarkers, TumorPLAC1 protein, humanPregnancy ProteinsCancerDevelopmentImmunotherapyPLAC1Placenta

Identifiers

PMID31165204
PMCPMC11028298
OpenAlexW2948407805

What OpenQuestion holds

Textmetadata
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.