Evidence map›Paper›PMID 41080449›Full record

ArticleBio-protocol2025

Standardized Culture of Skin Fibroblasts From Punch Biopsies for Germline DNA Isolation in Myeloid Malignancies: A Practical Bedside-to-Laboratory Approach.

Parampreet Kour, Nedhi Kumari, Naveen Kaushal, Tanvi Sharma, Shano Naseem, Jogeshwar Binota, Manupdesh Singh Sachdeva, Arihant Jain, Manish Rohilla, Reena Das and 2 more

Abstract read
In one paragraph

Article in Bio-protocol, 2025. 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
–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

1 citing paper in PubMed.

  1. Review
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

12 authors.

Parampreet KourDepartment of Haematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Nedhi KumariDepartment of Haematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Naveen KaushalDepartment of Biophysics, Panjab University, Chandigarh, India.
Tanvi SharmaDepartment of Biophysics, Panjab University, Chandigarh, India.
Shano NaseemDepartment of Haematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Jogeshwar BinotaDepartment of Haematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Manupdesh Singh SachdevaDepartment of Haematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Arihant JainDepartment of Clinical Hematology and Medical Oncology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Manish RohillaDepartment of Cytology and Gynaecological Pathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Reena DasDepartment of Haematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Pankaj MalhotraDepartment of Clinical Hematology and Medical Oncology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Pulkit RastogiDepartment of Haematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited germline variants are now recognized as important contributors to hematologic myeloid malignancies, but their reliable detection depends on obtaining uncontaminated germline DNA. In solid tumors, peripheral blood remains free of tumor cells and therefore serves as a standard source for germline testing. In contrast, peripheral blood often contains neoplastic or clonally mutated cells in hematologic malignancies, making it impossible to distinguish somatic from germline variants. This unique challenge necessitates using an alternative, non-hematopoietic tissue source for accurate germline assessment in patients with hematologic myeloid malignancies. Cultured skin fibroblasts derived from punch biopsies have long been considered the gold standard for this purpose. Nevertheless, most existing protocols are optimized for research settings and lack detailed, patient-centric workflows for routine clinical use. Addressing this translational gap, we present a robust, enzyme-free protocol for culturing dermal fibroblasts from skin punch biopsies collected at the bedside during routine bone marrow procedures. The method details practical bedside collection, sterile transport, mechanical dissection without enzymatic digestion, plating strategy, culture expansion, and high-yield DNA isolation with validated purity. By integrating this standardized approach into routine hematopathology workflows, the protocol ensures reliable germline material with minimal patient discomfort and a turnaround time suitable for clinical diagnostics. Key features • This protocol integrates bedside skin punch biopsy with routine bone marrow sampling to minimize patient discomfort and avoid additional invasive procedures. • It uses an optimized enzyme-free mechanical dissection method with fat removal, fine mincing, and scratched well plating to reduce contamination and improve fibroblast yield. • It provides an easy-to-follow workflow for primary fibroblast culture, plating, expansion, and harvest, suitable for routine hematopathology laboratories. • It consistently yields high-quality germline DNA free of hematopoietic contamination, ideal for genetic testing in myeloid malignancies.

Indexed as

Germline DNA isolationGermline predispositionMyeloid malignanciesPunch biopsySkin fibroblast culture

Identifiers

PMID41080449
PMCPMC12514132

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.