Schematic overview of the cellular and molecular mechanisms involved in the cancer progression, including the proposed cellular and molecular mechanisms in cancer cells trajectory. AT1: alveolar type 1 cells; AT2: alveolar type 2 cells; AAH: atypical adenomatous hyperplasia; AIS: adenocarcinoma in situ; MIA: minimally invasive adenocarcinoma; IA: invasive adenocarcinoma; EMT: epithelial-mesenchymal transition

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	Gene summary
	Malignant transformation analysis
	Malignant transformation related pathway analysis
	Cell-cell communication analysis
	Single-cell gene regulatory network inference analysis
	Somatic mutation of malignant transformation related genes
	Related drugs of malignant transformation related genes

Gene: SORL1

Gene summary for SORL1

Gene summary.

Gene information	Species	Human
	Gene symbol	SORL1
	Gene ID	6653
	Gene name	sortilin related receptor 1
	Gene Alias	C11orf32
	Cytomap	11q24.1
	Gene Type	protein-coding
	GO ID	GO:0000165
	UniProtAcc	A0A024R3H2

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Malignant transformation analysis

Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells

Malignant transformation involving gene list.

Entrez ID	Symbol	Replicates	Species	Organ	Tissue	Adj P-value	Log2FC	Malignancy
6653	SORL1	CA_HPV_2	Human	Cervix	CC	4.09e-02	-3.72e-01	0.0391
6653	SORL1	CA_HPV_3	Human	Cervix	CC	1.42e-09	-3.26e-01	0.0414
6653	SORL1	N_HPV_1	Human	Cervix	N_HPV	6.72e-06	-4.26e-01	0.0079
6653	SORL1	N_HPV_2	Human	Cervix	N_HPV	1.84e-02	-1.68e-01	-0.0131
6653	SORL1	CCI_1	Human	Cervix	CC	1.15e-03	-5.73e-01	0.528
6653	SORL1	CCII_1	Human	Cervix	CC	4.24e-11	-6.02e-01	0.3249
6653	SORL1	Tumor	Human	Cervix	CC	1.54e-07	-4.53e-01	0.1241
6653	SORL1	sample1	Human	Cervix	CC	2.76e-11	-6.14e-01	0.0959
6653	SORL1	sample3	Human	Cervix	CC	6.79e-09	-4.11e-01	0.1387
6653	SORL1	L1	Human	Cervix	CC	7.48e-07	-5.13e-01	0.0802
6653	SORL1	T1	Human	Cervix	CC	5.26e-19	-5.89e-01	0.0918
6653	SORL1	T3	Human	Cervix	CC	1.17e-06	-3.97e-01	0.1389
6653	SORL1	HTA11_1938_2000001011	Human	Colorectum	AD	1.38e-11	8.42e-01	-0.0811
6653	SORL1	HTA11_78_2000001011	Human	Colorectum	AD	1.85e-02	4.46e-01	-0.1088
6653	SORL1	HTA11_347_2000001011	Human	Colorectum	AD	1.62e-23	9.15e-01	-0.1954
6653	SORL1	HTA11_411_2000001011	Human	Colorectum	SER	1.41e-03	9.47e-01	-0.2602
6653	SORL1	HTA11_5212_2000001011	Human	Colorectum	AD	1.43e-03	6.84e-01	-0.2061
6653	SORL1	HTA11_6818_2000001021	Human	Colorectum	AD	4.15e-07	6.49e-01	0.0588
6653	SORL1	HTA11_99999965104_69814	Human	Colorectum	MSS	2.42e-04	5.47e-01	0.281
6653	SORL1	HTA11_99999971662_82457	Human	Colorectum	MSS	7.31e-07	6.56e-01	0.3859

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Transcriptomic changes along malignancy continuum.

Tissue	Expression Dynamics	Abbreviation
Cervix		CC: Cervix cancer
		HSIL_HPV: HPV-infected high-grade squamous intraepithelial lesions
		N_HPV: HPV-infected normal cervix
Colorectum (GSE201348)		FAP: Familial adenomatous polyposis
		CRC: Colorectal cancer
Colorectum (HTA11)		AD: Adenomas
		SER: Sessile serrated lesions
		MSI-H: Microsatellite-high colorectal cancer
		MSS: Microsatellite stable colorectal cancer
Esophagus		ESCC: Esophageal squamous cell carcinoma
		HGIN: High-grade intraepithelial neoplasias
		LGIN: Low-grade intraepithelial neoplasias
Liver		HCC: Hepatocellular carcinoma
		NAFLD: Non-alcoholic fatty liver disease
Lung		AAH: Atypical adenomatous hyperplasia
		AIS: Adenocarcinoma in situ
		IAC: Invasive lung adenocarcinoma
		MIA: Minimally invasive adenocarcinoma
Oral Cavity		EOLP: Erosive Oral lichen planus
		LP: leukoplakia
		NEOLP: Non-erosive oral lichen planus
		OSCC: Oral squamous cell carcinoma
Prostate		BPH: Benign Prostatic Hyperplasia
Skin		AK: Actinic keratosis
		cSCC: Cutaneous squamous cell carcinoma
		SCCIS:squamous cell carcinoma in situ

∗log2FC in expression of this searched gene in stem-like cells from each diseased tissue sample relative to stem-like cells in normal samples in each tissue plotted against the malignancy continuum. Samples are colored based on if they are from different disease stage.

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Malignant transformation related pathway analysis

Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer

Figure of enriched GO biological processes.

Tissue	Disease Stage	Enriched GO biological Processes
Colorectum	AD
Colorectum	SER
Colorectum	MSS
Colorectum	MSI-H
Colorectum	FAP

∗Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust).

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Enriched GO biological processes.

GO ID	Tissue	Disease Stage	Description	Gene Ratio	Bg Ratio	pvalue	p.adjust	Count
GO:009008317	Esophagus	ESCC	regulation of inclusion body assembly	14/8552	17/18723	2.22e-03	9.78e-03	14
GO:000181916	Esophagus	ESCC	positive regulation of cytokine production	244/8552	467/18723	2.29e-03	1.01e-02	244
GO:190121516	Esophagus	ESCC	negative regulation of neuron death	115/8552	208/18723	3.24e-03	1.34e-02	115
GO:00360106	Esophagus	ESCC	protein localization to endosome	18/8552	24/18723	3.43e-03	1.41e-02	18
GO:007084119	Esophagus	ESCC	inclusion body assembly	18/8552	24/18723	3.43e-03	1.41e-02	18
GO:19029597	Esophagus	ESCC	regulation of aspartic-type endopeptidase activity involved in amyloid precursor protein catabolic process	9/8552	10/18723	5.09e-03	1.92e-02	9
GO:001046620	Esophagus	ESCC	negative regulation of peptidase activity	140/8552	262/18723	6.73e-03	2.46e-02	140
GO:001095119	Esophagus	ESCC	negative regulation of endopeptidase activity	135/8552	252/18723	6.86e-03	2.51e-02	135
GO:00606281	Esophagus	ESCC	regulation of ER to Golgi vesicle-mediated transport	12/8552	15/18723	7.31e-03	2.63e-02	12
GO:00160427	Esophagus	ESCC	lipid catabolic process	168/8552	320/18723	7.97e-03	2.84e-02	168
GO:00708615	Esophagus	ESCC	regulation of protein exit from endoplasmic reticulum	19/8552	27/18723	8.35e-03	2.95e-02	19
GO:19052457	Esophagus	ESCC	regulation of aspartic-type peptidase activity	10/8552	12/18723	8.94e-03	3.12e-02	10
GO:00082869	Esophagus	ESCC	insulin receptor signaling pathway	66/8552	116/18723	9.76e-03	3.37e-02	66
GO:003424914	Esophagus	ESCC	negative regulation of cellular amide metabolic process	144/8552	273/18723	1.08e-02	3.67e-02	144
GO:00192168	Esophagus	ESCC	regulation of lipid metabolic process	172/8552	331/18723	1.20e-02	4.02e-02	172
GO:00434074	Esophagus	ESCC	negative regulation of MAP kinase activity	36/8552	59/18723	1.27e-02	4.21e-02	36
GO:00098967	Liver	NAFLD	positive regulation of catabolic process	108/1882	492/18723	2.68e-15	3.14e-12	108
GO:00421767	Liver	NAFLD	regulation of protein catabolic process	83/1882	391/18723	2.94e-11	1.01e-08	83
GO:00481936	Liver	NAFLD	Golgi vesicle transport	66/1882	296/18723	3.66e-10	9.30e-08	66
GO:00713755	Liver	NAFLD	cellular response to peptide hormone stimulus	65/1882	290/18723	3.95e-10	9.62e-08	65

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Enriched KEGG pathways.

Pathway ID

Tissue

Disease Stage

Description

Gene Ratio

Bg Ratio

pvalue

p.adjust

qvalue

Count

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Cell-cell communication analysis

Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states

Ligand

Receptor

LRpair

Pathway

Tissue

Disease Stage

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Single-cell gene regulatory network inference analysis

Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states

Cell Type

Tissue

Disease Stage

Target Gene

RSS

Regulon Activity

∗The dot plots of a searched regulon are shown for all cell subpopulations in each disease state of each tissue based on the regulon specific score inferred using pySCENIC and by calculating the average expression.

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Somatic mutation of malignant transformation related genes

Annotation of somatic variants for genes involved in malignant transformation

Hugo Symbol

Variant Class

Variant Classification

dbSNP RS

HGVSc

HGVSp

HGVSp Short

SWISSPROT

BIOTYPE

SIFT

PolyPhen

Tumor Sample Barcode

Tissue

Histology

Sex

Age

Stage

Therapy Types

Drugs

Outcome

SORL1

SNV

Missense_Mutation

novel

c.1999N>A

p.Asp667Asn

p.D667N

Q92673

protein_coding

deleterious(0)

probably_damaging(0.997)

TCGA-A8-A08H-01

Breast

breast invasive carcinoma

Female

>=65

I/II

Unknown

SORL1

SNV

Missense_Mutation

c.883N>A

p.Glu295Lys

p.E295K

Q92673

protein_coding

deleterious(0.02)

probably_damaging(0.989)

TCGA-AO-A0JC-01

Breast

breast invasive carcinoma

Female

<65

I/II

Chemotherapy

fluorouracil

SORL1

SNV

Missense_Mutation

novel

c.3388A>T

p.Thr1130Ser

p.T1130S

Q92673

protein_coding

tolerated(0.71)

benign(0.007)

TCGA-BH-A0E2-01

Breast

breast invasive carcinoma

Female

<65

III/IV

Chemotherapy

doxorubicin

SORL1

SNV

Missense_Mutation

novel

c.529N>C

p.Tyr177His

p.Y177H

Q92673

protein_coding

deleterious(0)

probably_damaging(0.996)

TCGA-BH-A18G-01

Breast

breast invasive carcinoma

Female

>=65

I/II

Unknown

SORL1

SNV

Missense_Mutation

c.1426C>T

p.His476Tyr

p.H476Y

Q92673

protein_coding

deleterious(0)

possibly_damaging(0.852)

TCGA-D8-A1XM-01

Breast

breast invasive carcinoma

Female

<65

I/II

Unknown

SORL1

SNV

Missense_Mutation

rs149445303

c.5627N>T

p.Thr1876Met

p.T1876M

Q92673

protein_coding

deleterious(0.01)

probably_damaging(0.997)

TCGA-E9-A243-01

Breast

breast invasive carcinoma

Female

<65

I/II

Chemotherapy

5-fluorouracil

SORL1

insertion

Frame_Shift_Ins

novel

c.4917_4918insATTGTTGGGATTCATCTCATTGTTATTTCTGTTACTCAAACCA

p.Asp1640IlefsTer60

p.D1640Ifs*60

Q92673

protein_coding

TCGA-A8-A07R-01

Breast

breast invasive carcinoma

Female

>=65

III/IV

Ancillary

zoledronic

SORL1

insertion

Frame_Shift_Ins

novel

c.2838_2839insTATTA

p.Thr947TyrfsTer2

p.T947Yfs*2

Q92673

protein_coding

TCGA-A8-A07U-01

Breast

breast invasive carcinoma

Female

>=65

III/IV

Chemotherapy

5-fluorouracil

SORL1

insertion

In_Frame_Ins

novel

c.4008_4009insCTGTATCAGATGGCACTCCCAGCGTGCCGTAGCCCCTTACCC

p.Val1336_Cys1337insLeuTyrGlnMetAlaLeuProAlaCysArgSerProLeuPro

p.V1336_C1337insLYQMALPACRSPLP

Q92673

protein_coding

TCGA-A8-A097-01

Breast

breast invasive carcinoma

Female

>=65

I/II

Hormone Therapy

tamoxiphen

SORL1

insertion

Frame_Shift_Ins

novel

c.5847_5848insTTTTGCAAATGTTCCGGTGCCCCTGCTGCTCTTGGAT

p.Ile1950PhefsTer20

p.I1950Ffs*20

Q92673

protein_coding

TCGA-B6-A0IM-01

Breast

breast invasive carcinoma

Female

>=65

I/II

Unknown

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Related drugs of malignant transformation related genes

Identification of chemicals and drugs interact with genes involved in malignant transfromation

(DGIdb 4.0)

Entrez ID

Symbol

Category

Interaction Types

Drug Claim Name

Drug Name

PMIDs

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