Evidence map›Paper›PMID 41933234›Full record

ReviewDiscover oncology2026

Emerging nanoimmunotherapeutic strategies for breast cancer.

Gauri Panzade, Atharva Anand Mahajan, Siva Parsad Panda, Ujjayita Chowdhury, Rohit Krishnan Iyer, Subhrojyoti Ghosh, Madhurima Koley, Akanksha Bhattacharya, Avishek Chatterjee, Anuvab Dey and 10 more

Abstract readReview
In one paragraph

Review in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

20 authors.

Gauri Panzade *Advance Centre for Treatment Research and Education in Cancer, Navi Mumbai, Maharashtra, India.
Atharva Anand Mahajan *Advance Centre for Treatment Research and Education in Cancer, Navi Mumbai, Maharashtra, India.
Siva Parsad PandaInstitute of Pharmaceutical Research, GLA University, Mathura, Uttar Pradesh, 281406, India.
Ujjayita ChowdhuryAdvance Centre for Treatment Research and Education in Cancer, Navi Mumbai, Maharashtra, India.
Rohit Krishnan IyerAdvance Centre for Treatment Research and Education in Cancer, Navi Mumbai, Maharashtra, India.
Subhrojyoti GhoshInfection Biology Group, Centre for Cellular and Molecular Biology, Hyderabad, Telangana, India.
Madhurima KoleyDepartment of Biosciences and Bioengineering, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand, India.
Akanksha BhattacharyaDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), Bhopal, Madhya Pradesh, India.
Avishek ChatterjeeDepartment of Biotechnology, Indian Institute of Technology Madras, Chennai, Tamil Nadu, India.
Anuvab DeyDepartment of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, Assam, India.
Chandrika SarkarDepartment of Biotechnology, Indian Institute of Technology Madras, Chennai, Tamil Nadu, India.
Ankita ChowdhuryDepartment of Biochemical Engineering and Biotechnology, Indian Institute of Technology Delhi, Hauz Khas, New Delhi, Delhi, India.
Bhaskarjyaa ChatterjeeDepartment of Biotechnology, Anna University, Chennai, Tamil Nadu, India.
Souvadra DasSchool of Nano Science and Technology, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India.
Shrimanti DasDepartment of Biotechnology, Heritage Institute of Technology, Kolkata, India.
Souhardya BandyopadhyaySchool of Biosciences and Bioengineering, Indian Institute of Technology Mandi, Mandi, Himachal Pradesh, India.
Ramya Lakshmi RajendranBK21 FOUR KNU Convergence Educational Program of Biomedical Sciences for Creative Future Talents, Kyungpook National University, Department of Biomedical Sciences, School of Medicine, Daegu, 41944, Republic of Korea. ramyag@knu.ac.kr.
Prakash GangadaranDepartment of Nuclear Medicine, School of Medicine, Kyungpook National University, Daegu, 41944, Republic of Korea. prakashg@knu.ac.kr.
Byeong-Cheol AhnBK21 FOUR KNU Convergence Educational Program of Biomedical Sciences for Creative Future Talents, Kyungpook National University, Department of Biomedical Sciences, School of Medicine, Daegu, 41944, Republic of Korea. abc2000@knu.ac.kr.
Saurabh Kumar JhaDepartment of Zoology, Kalindi College, University of Delhi, New Delhi, 110008, India. Jhasaurabh017@gmail.com.

Funding

National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) NRF-2022R1A2C2005057
6 · The paper itself

Abstract

Breast cancer is among the most prevalent forms of cancer. The conventional modalities employed in the management of breast cancer include mainly surgery, radiation, and chemotherapy. The enhanced comprehension of the complex pathobiology of breast cancer has resulted in the emergence of immunotherapy as a highly auspicious therapeutic approach. This is a narrative review focusing on nanotechnology‑enabled immunotherapy strategies for breast cancer, at the interface of tumor immunology and nanomedicine. We highlight lipid nanoparticles, polymeric nanoparticles, inorganic nanomaterials, virus-like particles, and extracellular vesicle-based systems that modulate the anti-tumor immune response. Immunotherapy stimulates the patient's immune system to selectively recognize and eliminate cancerous cells. The present methodology focuses on the primary molecular constituents of neoplastic tissue and offers a potentially novel therapeutic strategy. Comprehending the intricate interplay between neoplastic cells and immunological components is paramount for devising efficacious therapeutic interventions. Immunotherapy can not only eliminate tumors but also be proven effective in impeding metastasis and recurrence. The implementation of immunotherapy in clinical settings has encountered certain constraints, such as weak immune responses resulting from insufficient delivery of immunostimulants to target cells and unregulated modulation of the immune system, leading to the development of autoimmunity and non-specific inflammation. Nanomedicines offer a unique opportunity to maximize the efficacy of immunotherapy and significantly reduce its side effects. The present article discusses the latest developments in breast cancer immunotherapy involving nanotechnology. These advancements encompass a range of approaches, including the direct stimulation of the immune system via the administration of tumor antigens and adjuvants to immune cells, the modification of the tumor microenvironment to reduce immunosuppression, and integration with other therapeutic modalities. We summarise current evidence, identify critical knowledge gaps, and outline future directions for biomarker-guided and combination nano-immunotherapy trials in breast cancer.

Indexed as

Breast cancerImmunomodulationImmunotherapyNanomedicineResistance

Identifiers

PMID41933234
PMCPMC13172157

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.