Evidence map›Paper›PMID 42853456›Full record

ArticleEndocrine pathology2026

Distinct Molecular Pathways Driving Thymic and Pulmonary Neuroendocrine Neoplasms: Organ of Origin Defines Molecular Identity and Yields CD44 as a Marker of Pulmonary Neuroendocrine Tumors.

Hanibal Bohnenberger, Stefan Küffer, Arber Qoku, Julius Bodemeyer, Nelia Nause, Björn Häupl, Kirsten Reuter-Jessen, Tessa Rosenthal, Linja Feldmann, Katharina Ofner and 16 more

Abstract read
PubMed Publisher
In one paragraph

Article in Endocrine pathology, 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

26 authors.

Hanibal BohnenbergerInstitute of Pathology, University Medical Center Göttingen, Robert-Koch-Str. 40, Göttingen, D-37075, Germany.
Stefan KüfferInstitute of Pathology, University Medical Center Göttingen, Robert-Koch-Str. 40, Göttingen, D-37075, Germany.
Arber QokuGoethe University Frankfurt, Frankfurt am Main, Germany.
Julius BodemeyerInstitute of Pathology, University Medical Center Göttingen, Robert-Koch-Str. 40, Göttingen, D-37075, Germany.
Nelia NauseComprehensive Cancer Center Göttingen (G-CCC), University Medical Center Göttingen, Göttingen, Germany.
Björn HäuplDepartment of Medicine II, Hematology/Oncology, Goethe University, Frankfurt, Germany.
Kirsten Reuter-JessenInstitute of Pathology, University Medical Center Göttingen, Robert-Koch-Str. 40, Göttingen, D-37075, Germany.
Tessa RosenthalInstitute of Pathology, University Medical Center Göttingen, Robert-Koch-Str. 40, Göttingen, D-37075, Germany.
Linja FeldmannInstitute of Pathology, University Medical Center Göttingen, Robert-Koch-Str. 40, Göttingen, D-37075, Germany.
Katharina OfnerInstitute of Pathology, University Medical Center Göttingen, Robert-Koch-Str. 40, Göttingen, D-37075, Germany.
Daniela FrancesBioanalytical Mass Spectrometry Group, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
Celia VogelBioanalytical Mass Spectrometry Group, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
Christof LenzInstitute of Pathology, University Medical Center Göttingen, Robert-Koch-Str. 40, Göttingen, D-37075, Germany.
Moritz JesinghausDepartment of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center, Göttingen, Germany.
Omar ElakadInstitute of Pathology, University Medical Center Göttingen, Robert-Koch-Str. 40, Göttingen, D-37075, Germany.
Denise MüllerInstitute of Pathology, University Medical Center Göttingen, Robert-Koch-Str. 40, Göttingen, D-37075, Germany.
Alexander Otto KönigDepartment of Hematology and Medical Oncology, University Medical Center Göttingen, Göttingen, Germany.
Tobias R OverbeckDepartment of Thoracic and Cardiovascular Surgery, University Medical Center, Georg-August University, Göttingen, Germany.
Alexander von Hammerstein-EquordDepartment of Thoracic Surgery, Lungenklinik Hemer, Hemer, Germany.
Marc HinterthanerDepartment of Thoracic Surgery, Lungenklinik Hemer, Hemer, Germany.
Stefan WelterDepartment of Thoracic Surgery, Lungenklinik Hemer, Hemer, Germany.
Henning UrlaubInstitute of Pathology, University Medical Center Göttingen, Robert-Koch-Str. 40, Göttingen, D-37075, Germany.
Florian BuettnerGoethe University Frankfurt, Frankfurt am Main, Germany.
Thomas OellerichDepartment of Medicine II, Hematology/Oncology, Goethe University, Frankfurt, Germany.
Alexander MarxInstitute of Pathology, University Medical Center Göttingen, Robert-Koch-Str. 40, Göttingen, D-37075, Germany.
Philipp StröbelInstitute of Pathology, University Medical Center Göttingen, Robert-Koch-Str. 40, Göttingen, D-37075, Germany. philipp.stroebel@med.uni-goettingen.de.ORCID https://orcid.org/0000-0002-8528-8060

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thymic and pulmonary neuroendocrine neoplasms (NEN) are morphologically similar but arise from different embryonic tissues. Whether this similarity extends to shared molecular programs is unclear. We compared 45 thymic and 37 pulmonary NEN by immunohistochemistry, targeted and exome sequencing, NanoString RNA profiling and mass spectrometry-based proteomics. The RNA and proteomic profiles of pulmonary and thymic neuroendocrine tumors (LuNET and TNET) were clearly different, while the profiles of neuroendocrine carcinomas of both organs (LuNEC and TNEC) were largely overlapping. A subgroup of TNET corresponding to NET G3 clustered with lower-grade thymic NET rather than NEC. NET of both organs showed a low mutational burden and were proliferatively quiescent but diverged metabolically: LuNET showed broad metabolic and stress signaling and TNET a quiescent phenotype with PI3K/AKT/mTOR as the only enriched pathway. NEC of both organs converged on cell cycle activation and metabolic depletion with frequent TP53 and RB1 co-inactivation, but diverged immunologically: LuNEC were immune-hot, whereas TNEC showed epithelial-mesenchymal transition and a markedly lower mutational burden. CD44 stood out in both the transcriptomic and the proteomic analysis and was therefore immunohistochemically validated in an independent, larger cohort that included also gastrointestinal and pancreatic tumors. CD44 was high in pulmonary NET and low in every other subgroup (p = 2.1 × 10⁻¹³), identifying it as a new complementary marker of pulmonary origin. In summary, thoracic NEN segregate by anatomical origin as well as by differentiation grade. Wether these differences require treatments adapted to the organ of origin remains to be established.

Indexed as

Biomarkers, TumorHyaluronan ReceptorsLung NeoplasmsNeuroendocrine TumorsThymus NeoplasmsHumansImmunohistochemistryProteomicsSignal TransductionBiomarkers, TumorCD44 protein, humanHyaluronan ReceptorsMulti-omicsPathologyProteomicsPulmonary neuroendocrine neoplasmsThymic neuroendocrine neoplasms

Identifiers

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.