Evidence map›Paper›PMID 41497695›Full record

ArticleWorld journal of experimental medicine2025

Lack of cytoplasmic expression of a new marker programmed cell death ligand-1 in tumor cells is significant.

Marina A Senchukova, Evgeniya Yu Zubareva, Natalia V Saidler, Lyubov V Krivolapova

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Article in World journal of experimental medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Marina A SenchukovaScientific and Clinical Center No. 3, Petrovsky National Research Centre of Surgery, Moscow 108840, Troitsk, Russia. masenchukova@yandex.com.
Evgeniya Yu ZubarevaDepartment of Oncology, Orenburg State Medical University, Orenburg 460021, Orenburgskaya Oblast', Russia.
Natalia V SaidlerDepartment of Pathology, Orenburg Regional Cancer Clinic, Orenburg 460021, Orenburgskaya Oblast', Russia.
Lyubov V KrivolapovaScientific and Clinical Center No. 2, Petrovsky National Research Centre of Surgery, Moscow 117953, Moskva, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent studies have indicated that an antibody against programmed cell death protein 1-ligand 1 (PDCD1-LG1), a new marker of programmed cell death-ligand 1 expression, is promising for studying the mechanisms of breast cancer (BC) progression and resistance to chemotherapy.

aimTo compare the features of PDCD1-LG1 expression in chemoresistant luminal A BC and BC with high Ki67 indices.

methodsThis prospective single-center observational cohort study included 148 patients with newly diagnosed primary resectable BC. The tumor sections were stained with antibodies against PDCD1-LG1. The statistical calculations were performed using Statistica software version 12.0.

resultsCytoplasmic PDCD1-LG1 (cPDCD1-LG1) expression was detected in the nonneoplastic epithelium, tumor cells (TCs) and immune cells (ICs). A lack of cPDCD1-LG1 expression in ≥ 20% of TCs and a PDCD1-LG1+ IC score ≥ 10% were associated with aggressive BC characteristics, including tumor G3, estrogen receptor-negative status, overexpression of human epidermal growth factor receptor 2 (HER2+), luminal B HER2+ BC, nonluminal HER2+ BC and triple-negative BC. The lack of cPDCD1-LG1 expression in < 20% of the TCs, in combination with a PDCD1-LG1+ IC score < 10% and G1, was characteristic of chemoresistant luminal A BC, whereas the lack of cPDCD1-LG1 expression in ≥ 20% of the TCs, combined with a PDCD1-LG1+ IC score ≥ 10%, was a predictor of high BC sensitivity to chemotherapy.

conclusionThese results indicate that both the lack of cPDCD1 LG1 in TCs and the PDCD1 LG1 IC score and their combination may be important for assessing BC prognosis and sensitivity to chemotherapy.

Indexed as

Breast cancerChemoresistanceProgrammed cell death protein 1-ligand 1Programmed death-ligand 1Сytoplasmic programmed cell death protein 1 ligand 1

Identifiers

PMID41497695
PMCPMC12767143

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