Evidence map›Paper›PMID 40214413›Full record

ArticleInternational journal of cancer2025

Human sporadic breast carcinoma histotypes driven by the Human Betaretrovirus homologous to Mouse Mammary Tumor Virus.

Prospero Civita, Chiara Maria Mazzanti, Francesca Lessi, Caterina Marchiò, Cristian Scatena, Michele Menicagli, Matteo Ghilli, Manuela Roncella, Antonio Giuseppe Naccarato, Anna Sapino and 3 more

Abstract read
In one paragraph

Article in International journal of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. 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

13 authors.

Prospero CivitaFondazione Pisana per la Scienza, San Giuliano Terme, Pisa, Italy.ORCID 0000-0002-8313-1094
Chiara Maria MazzantiFondazione Pisana per la Scienza, San Giuliano Terme, Pisa, Italy.ORCID 0000-0002-7249-9221
Francesca LessiFondazione Pisana per la Scienza, San Giuliano Terme, Pisa, Italy.ORCID 0000-0002-9766-8511
Caterina MarchiòDepartment of Medical Science, University of Turin, Turin, Italy.ORCID 0000-0003-2024-6131
Cristian ScatenaDepartment of Translational Research and New Technologies in Medicine, University of Pisa, Pisa, Italy.ORCID 0000-0002-4862-0845
Michele MenicagliFondazione Pisana per la Scienza, San Giuliano Terme, Pisa, Italy.
Matteo GhilliBreast Cancer Center, Pisa University Hospital, Pisa, Italy.ORCID 0000-0001-5536-7377
Manuela RoncellaBreast Cancer Center, Pisa University Hospital, Pisa, Italy.ORCID 0000-0002-1452-2155
Antonio Giuseppe NaccaratoDepartment of Translational Research and New Technologies in Medicine, University of Pisa, Pisa, Italy.ORCID 0000-0002-8195-9445
Anna SapinoDepartment of Medical Science, University of Turin, Turin, Italy.ORCID 0000-0003-3542-9571
Jacob HochmanAlexander Silberman Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem, Israel.ORCID 0000-0003-4203-3276
Mauro PistelloDepartment of Translational Research and New Technologies in Medicine, University of Pisa, Pisa, Italy.ORCID 0000-0003-0908-6253
Generoso BevilacquaDepartment of Translational Research and New Technologies in Medicine, University of Pisa, Pisa, Italy.ORCID 0000-0001-8857-2609

Funding

Ministero della Salute - Italian Ministry of Health. Next Generation EU - PNRR M6C2 - Investimento 2.1 Valorizzazione e potenziamento della ricerca biomedica del SSN (Codice progetto PNRR-MAD-2022-12376570, CAP: PNRR0308, CDC: 03080103, UDP: 0308PNRR-FONDI NEXTGENERATIONEU) 03080103Ministero della Salute - Italian Ministry of Health. Next Generation EU - PNRR M6C2 - Investimento 2.1 Valorizzazione e potenziamento della ricerca biomedica del SSN (Codice progetto PNRR-MAD-2022-12376570, CAP: PNRR0308, CDC: 03080103, UDP: 0308PNRR-FONDI NEXTGENERATIONEU) 0308PNRR-FONDINEXTGENERATIONEUMinistero della Salute - Italian Ministry of Health. Next Generation EU - PNRR M6C2 - Investimento 2.1 Valorizzazione e potenziamento della ricerca biomedica del SSN (Codice progetto PNRR-MAD-2022-12376570, CAP: PNRR0308, CDC: 03080103, UDP: 0308PNRR-FONDI NEXTGENERATIONEU) PNRR0308Ministero della Salute - Italian Ministry of Health. Next Generation EU - PNRR M6C2 - Investimento 2.1 Valorizzazione e potenziamento della ricerca biomedica del SSN (Codice progetto PNRR-MAD-2022-12376570, CAP: PNRR0308, CDC: 03080103, UDP: 0308PNRR-FONDI NEXTGENERATIONEU) PNRR-MAD-2022-12376570
6 · The paper itself

Abstract

The viral hypothesis for human sporadic breast carcinoma is based on the murine model of Mouse Mammary Tumor Virus (MMTV)-induced mammary tumors. Known risk factors like estrogens, obesity, and alcohol do not play a direct causal role. The Human Betaretrovirus (HBRV), also called Human Mammary Tumor Virus (HMTV), is the human homolog of MMTV, implicated in sporadic breast carcinoma (80% of ductal carcinoma in situ and 40% of invasive tumors). In contrast, hereditary breast carcinomas lack viral sequences. Murine mammary tumor histotypes are determined by specific viral strains activating definite molecular pathways via insertional mutagenesis. Similarly, the diverse histotypes observed in human invasive breast carcinoma may be influenced by a viral etiology. A study of 253 invasive breast carcinoma cases, representing 15 histotypes, detected HBRV/MMTV-ENV sequences in 20%, consistent with international literature. All histotypes tested positive except those linked to hereditary syndromes, such as medullary, apocrine, and metaplastic carcinoma. This distinction reinforces the reported lack of association between HBRV/HMTV and hereditary breast cancer, while supporting a viral etiology for sporadic carcinoma. Relevant characteristics of sporadic histotypes align with the "hit and run" hypothesis of viral carcinogenesis. Histotype differences may result from molecular pathways activated by Int genes, though mechanism beyond insertional mutagenesis and the possibility of specific HBRV strains cannot be ruled out. The potential for detected viral sequences to originate in human tumors from endogenous MMTV or contamination with murine material is critically examined.

Indexed as

BetaretrovirusBreast NeoplasmsMammary Tumor Virus, MouseAnimalsFemaleHumansMiceRetroviridae Infectionsbreast cancer etiologybreast cancer histotypehuman betaretrovirus‐HBRVhuman mammary tumor virus‐HMTVmouse mammary tumor virus‐MMTV

Identifiers

PMID40214413
PMCPMC12079628

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Registered trials

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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.