Pan-cancer Transcriptomic Predictors of Perineural Invasion Improve Occult Histopathologic Detection

Purpose: Perineural invasion (PNI) is associated with aggressive tumor behavior, recurrence, and metastasis, and can influence the administration of adjuvant treatment. However, standard histopathologic examination has limited sensitivity in detecting PNI and does not provide insights into its mechanistic underpinnings. Experimental Design: A multivariate Cox regression was performed to validate associations between PNI and survival in 2,029 patients across 12 cancer types. Differential expression and gene set enrichment analysis were used to learn PNI-associated programs. Machine learning models were applied to build a PNI gene expression classifier. A blinded re-review of hematoxylin and eosin (H&E) slides by a board-certified pathologist helped determine whether the classifier could improve occult histopathologic detection of PNI. Results: PNI associated with both poor overall survival [HR, 1.73; 95% confidence interval (CI), 1.27–2.36; P < 0.001] and disease-free survival (HR, 1.79; 95% CI, 1.38–2.32; P < 0.001). Neural-like, prosurvival, and invasive programs were enriched in PNI-positive tumors (Padj < 0.001). Although PNI-associated features likely reflect in part the increased presence of nerves, many differentially expressed genes mapped specifically to malignant cells from single-cell atlases. A PNI gene expression classifier was derived using random forest and evaluated as a tool for occult histopathologic detection. On a blinded H&E re-review of sections initially described as PNI negative, more specimens were reannotated as PNI positive in the high classifier score cohort compared with the low-scoring cohort (P = 0.03, Fisher exact test). Conclusions: This study provides salient biological insights regarding PNI and demonstrates a role for gene expression classifiers to augment detection of histopathologic features.

[1]  Gabriella A. Conte,et al.  S100 Staining Adds to the Prognostic Significance of the Combination of Perineural Invasion and Lymphovascular Invasion in Colorectal Cancer , 2020, Applied immunohistochemistry & molecular morphology : AIMM.

[2]  Perineural Invasion , 2020, Definitions.

[3]  F. Jamali,et al.  Single dose pharmacokinetics and bioavailability of glucosamine in the rat. , 2002, Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques.

[4]  P. Frenette,et al.  Nerves in cancer , 2020, Nature Reviews Cancer.

[5]  T. Kuner,et al.  Glutamatergic synaptic input to glioma cells drives brain tumour progression , 2019, Nature.

[6]  J. Werner,et al.  Cholinergic Signaling via Muscarinic Receptors Directly and Indirectly Suppresses Pancreatic Tumorigenesis and Cancer Stemness. , 2018, Cancer discovery.

[7]  Arul M. Chinnaiyan,et al.  Cancer transcriptome profiling at the juncture of clinical translation , 2017, Nature Reviews Genetics.

[8]  Mikael Benson,et al.  Single-cell analyses to tailor treatments , 2017, Science Translational Medicine.

[9]  L. J. K. Wee,et al.  Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors , 2017, Nature Genetics.

[10]  H. Su,et al.  Perineural Invasion and TAMs in Pancreatic Ductal Adenocarcinomas: Review of the Original Pathology Reports Using Immunohistochemical Enhancement and Relationships with Clinicopathological Features , 2014, Journal of Cancer.

[11]  Benjamin E. Gross,et al.  Integrative Analysis of Complex Cancer Genomics and Clinical Profiles Using the cBioPortal , 2013, Science Signaling.

[12]  Benjamin E. Gross,et al.  The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data. , 2012, Cancer discovery.

[13]  G. Hostetter,et al.  Perineural invasion and associated pain in pancreatic cancer , 2011, Nature Reviews Cancer.

[14]  A. Yılmaz,et al.  Clinical impact of visceral pleural, lymphovascular and perineural invasion in completely resected non-small cell lung cancer. , 2011, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[15]  H. Ha,et al.  Clinical significance of CXCL16/CXCR6 expression in patients with prostate cancer. , 2011, Molecular medicine reports.

[16]  Michael R Stratton,et al.  Genomics and the continuum of cancer care. , 2011, The New England journal of medicine.

[17]  S. Gabriel,et al.  Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1. , 2010, Cancer cell.

[18]  George A. Calin,et al.  Expression of microRNAs and protein‐coding genes associated with perineural invasion in prostate cancer , 2008, The Prostate.

[19]  T. Wheeler,et al.  Enhanced survival in perineural invasion of pancreatic cancer: an in vitro approach. , 2007, Human pathology.

[20]  H. Hoffman,et al.  Perineural and vascular invasion in oral cavity squamous carcinoma: increased incidence on re-review of slides and by using immunohistochemical enhancement. , 2005, Archives of pathology & laboratory medicine.

[21]  T. Wheeler,et al.  Growth and Survival Mechanisms Associated with Perineural Invasion in Prostate Cancer , 2004, Cancer Research.

[22]  M. Kattan,et al.  Prognostic significance of the diameter of perineural invasion in radical prostatectomy specimens. , 2001, Human pathology.

[23]  L. Liotta,et al.  General mechanisms of metastasis , 1997, Cancer.

[24]  An Adrenergic-Neurotrophin Feedforward Loop Promotes Pancreatic Cancer. , 2018, Cancer discovery.

[25]  Arul M Chinnaiyan,et al.  Translating cancer genomes and transcriptomes for precision oncology , 2016, CA: a cancer journal for clinicians.

[26]  L. Kowalski,et al.  Prognostic impact of perineural invasion and lymphovascular invasion in advanced stage oral squamous cell carcinoma. , 2015, International journal of oral and maxillofacial surgery.

[27]  A. R.,et al.  Review of literature , 1969, American Potato Journal.