Secretory phenotype

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Unknown (1905)
Genomics (603)
Transcriptomics (580)
Proteomics (105)
Other (18)
Metabolomics (5)
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Models (3)

Organisms

Homo sapiens (402)
Mus musculus (239)
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Organisms

Homo sapiens (278)
Mus musculus (160)
Rattus norvegicus (11)
Callithrix jacchus (2)
Candida albicans (2)
Arabidopsis thaliana (2)
Mus musculus isatissus (1)
Komagataella phaffii GS115 (1)
Mesocricetus auratus (1)
Mus (1)
Macaca mulatta (1)
Schizosaccharomyces pombe (1)
Drosophila melanogaster (1)
Gallus gallus (1)
human metagenome (1)
Caenorhabditis elegans (1)
Danio rerio (1)

Repository

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Tissue

Cell culture (22)
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Colorectal cancer (1)
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Melanoma (1)
Neuroblastoma (1)
Obesity (1)
Osteosarcoma (1)
Pancreatic ductal adenocarcinoma (1)
Severe acute respiratory syndrome (1)
Sjogren's Syndrome (1)

Technology Type

Mass Spectrometry (66)
Shotgun proteomics (39)
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Instrument Platform

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6560 Q-TOF LC/MS (2)
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HPC (1)
NEXTflex small RNA library preparation kit v4; TruSeq exome RNA library preparation kit (Illumina); High Sensitivity DNA ScreenTape D1000 (1)
QIAzol and miRNeasy micro kits; Bioanalyzer TapeStation 2100; Qubit microRNA assay (1)
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None (1)
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Instrument (1)
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Publication Date

2025 (124)
2026 (89)
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2023 (66)
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2014 (49)
2013 (41)
2020 (34)
2012 (23)
2016 (22)
2015 (22)
2019 (18)
2010 (18)
2011 (16)
2018 (15)
2009 (11)
2008 (10)
2007 (9)
2017 (7)
2005 (7)
2004 (2)
2003 (1)
2006 (1)

CHEBI ID

CHEBI:17822 (2)
CHEBI:26271 (2)
CHEBI:22660 (2)
CHEBI:27570 (2)
CHEBI:18186 (2)
CHEBI:26986 (2)
CHEBI:16811 (2)
CHEBI:24898 (2)
CHEBI:25017 (2)
CHEBI:28044 (2)
CHEBI:27266 (2)
CHEBI:29016 (2)
CHEBI:25094 (2)
CHEBI:18237 (2)
CHEBI:78320 (2)
CHEBI:15428 (2)
CHEBI:16614 (1)
CHEBI:16613 (1)
CHEBI:16612 (1)
CHEBI:16611 (1)
CHEBI:26562 (1)
CHEBI:22193 (1)
CHEBI:52330 (1)
CHEBI:16615 (1)
CHEBI:17665 (1)
CHEBI:28315 (1)
CHEBI:18240 (1)
CHEBI:17768 (1)
CHEBI:36006 (1)
CHEBI:73061 (1)

Metabolite Name

Spermidine M+05 (1)
Spermidine M+04 (1)
Spermidine M+03 (1)
Spermidine M+02 (1)
Spermidine M+01 (1)
Spermidine M+00 (1)
Putrescine M+04 (1)
Putrescine M+03 (1)
Putrescine M+02 (1)
Putrescine M+01 (1)
Putrescine M+00 (1)
N-Acetylspermidine M+05 (1)
N-Acetylspermidine M+04 (1)
N-Acetylspermidine M+03 (1)
N-Acetylspermidine M+02 (1)
N-Acetylspermidine M+01 (1)
N-Acetylspermidine M+00 (1)
N-Acetylputrescine M+05 (1)
N-Acetylputrescine M+04 (1)
N-Acetylputrescine M+03 (1)
N-Acetylputrescine M+02 (1)
N-Acetylputrescine M+01 (1)
N-Acetylputrescine M+00 (1)
Glycerophosphorylcholine (1)
Glycerophosphatidylethanolamine (1)
Unknown 1 (1)
Uridine diphosphate galactose (1)
D-Sedoheptulose-7-phosphate (1)
Ribose phosphate (1)
PEP (1)

IsPrivate

False (2)

First Public Date

2026 (99)
2025 (99)
2024 (84)
2023 (57)
2021 (46)
2022 (42)
2014 (33)
2020 (24)
2019 (12)
2018 (11)
2016 (9)
2017 (5)
2015 (3)
2013 (3)

Classification

fungi (2)

Study type

Transcription profiling by array (150)
RNA-seq of coding RNA (23)
ChIP-seq (8)
RNA-seq of coding RNA from single cells (6)
Unknown experiment type (4)
Other (3)
Comparative genomic hybridization by array (2)
DNA-seq (2)
Transcription profiling by SAGE (1)
Animal - Single-cell sequencing (1)
Human - One-color microarray (1)
Transcription profiling by RT-PCR (1)
RIP-seq (1)
MicroRNA profiling by array (1)
RNA-seq of non coding RNA (1)

Release Date

2025 (272)
2023 (241)
2022 (233)
2024 (219)
2021 (167)
2020 (151)
2019 (120)
2018 (91)
2014 (84)
2016 (79)
2017 (73)
2015 (69)
2013 (60)
2026 (54)
2011 (37)
2012 (36)
2010 (33)
2008 (22)
2009 (18)
2007 (13)
2005 (12)
2004 (6)
2003 (4)
2006 (4)
1999 (4)
2001 (3)
1998 (3)
2000 (1)
1997 (1)

Lab affiliation

Human Phenome Institute,Zhangjiang FudanInternational Innovation Center, Fudan UniversityShanghai, 201203, China. (2)
School of Biomedical Sciences, Faculty of Medicine and Health, UNSW Sydney (2)
School of Medicine, University College Dublin, Belfield, Dublin 4, Ireland (2)
1. Competence Centre on Health Technologies, Tiigi 61b, Tartu, Estonia 2. Chair of Obstetrics and Gynaecology, Institute of Biomedicine, University of Tartu, Ravila 19, Tartu, Estonia (1)
Analytical Biochemistry and Proteomics Unit, Institut Pasteur de Montevideo and Instituto de Investigaciones Biológicas Clemente Estable (1)
Associate professor at University of Campinas-SP (UNICAMP-SP) (1)
Biomedical Research Center, University Hospital Hradec Kralove, Czech Republic (1)
Biotech Research and Innovation Centre, University of Copenhagen, Ole Maaløes Vej 5, Copenhagen 2200, Denmark (1)
CAS（Chinese Academy of Sciences） (1)
Centre for Applied Bioanthropology, Institute for Anthropological Research, Zagreb, Croatia (1)
Charles Perkins Centre, School of Medical Sciences, University of Sydney, Sydney, Australia. (1)
Department Of Pharmacy (1)
Department of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461, United States (1)
Department of Biochemistry, Center for Biomedical Mass Spectrometry, Boston University School of Medicine, Boston, MA 02118, USA (1)
Department of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, 87# Xiangya Road, Changsha, Hunan 410008, PR China (1)
Department of Experimental Oncology, IEO, European Institute of Oncology IRCCS, Milan 20139, Italy (1)
Department of Genome Integrity, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic (1)
Department of Neurosurgery, Chongqing Research Center for Glioma Precision Medicine, Chongqing General Hospital, Chongqing University (1)
Department of Pharmacology and Lineberger Comprehensive Cancer Center at University of North Carolina at Chapel Hill (1)
Department of Pharmacology, Tianjin Key Laboratory of Inflammatory Biology, The Province and Ministry Co-sponsored Collaborative Innovation Center for Medical Epigenetics, Key Laboratory of Experimental Hematology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China. (1)
Department of Psychiatry, Oregon Health & Science University, Portland, OR (1)
Department of Veterinary Medicine and Animal Sciences (DIVAS), University of Milano (1)
Department of Zoology, School of Natural Sciences, National University of Ireland, Galway. (1)
Division of Endocrinology, Metabolism & Lipid Research, Washington University, St. Louis Department of Cell Biology & Physiology, Washington University, St. Louis (1)
Division of Obstetrics and Gynecology, Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institutet, 14186 Stockholm, Sweden (1)
EDyP (1)
European Institute of Oncology IRCCS, 20139 Milan, Italy (1)
Genome and Stem Cell Center, Erciyes University, Turkiye (1)
Genomics Research Center, Academia Sinica, Taipei, Taiwan. Drug Development Center, China Medical University, Taichung, Taiwan. Department of Biological Chemistry, University of California, Irvine. (1)
Head of the Curie Institute Mass Spectrometry Platform (1)

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MLL1 is essential for the senescence-associated secretory phenotype

This SuperSeries is composed of the SubSeries listed below. Oncogene-induced senescence (OIS) and therapy-induced senescence (TIS), while tumor-suppressive, also promote procarcinogenic effects by activating the DNA damage response (DDR), which in turn induces inflammation. This inflammatory respon...

ORGANISM(S): Homo sapiens

2016-02-22 | E-GEOD-78142 | biostudies-arrayexpress

MLL1 is essential for the senescence-associated secretory phenotype [ChIP-Seq]

Oncogene-induced senescence (OIS) and therapy-induced senescence (TIS), while tumor-suppressive, also promote procarcinogenic effects by activating the DNA damage response (DDR), which in turn induces inflammation. This inflammatory response prominently includes an array of cytokines known as the se...

ORGANISM(S): Homo sapiens

2016-02-23 | E-GEOD-78141 | biostudies-arrayexpress

MLL1 is essential for the senescence-associated secretory phenotype [RNA-Seq]

ORGANISM(S): Homo sapiens

2016-02-23 | E-GEOD-78138 | biostudies-arrayexpress

Senescence Associated Secretory Phenotype

Cells and tissues are exposed to stress from numerous sources. Senescence is a protective mechanism that prevents malignant tissue changes and constitutes a fundamental mechanism of aging. It can be accompanied by a senescence associated secretory phenotype (SASP) that causes chronic inflammation. W...

11863 | Cell Collective

Characterization of intact proteomic profile of senescent-associated secretory phenotype (SASP) by top-down mass spectrometry.

Senescent cells are increasingly recognized as major contributors to age-related diseases, primarily through the secretion of bioactive molecules known as the senescence-associated secretory phenotype (SASP). The SASP plays a crucial role in promoting various age-related conditions, including neurod...

ORGANISM(S): Homo sapiens (Human)

2025-12-29 | PXD061829 | Pride