Jump to content

User:Aarondeworld/sandbox

From Wikipedia, the free encyclopedia

hPG80 refers to the extracellular and oncogenic version of progastrin. This name first appeared in a scientific publication in January 2020[1]. Until that date, scientific publications only mention progastrin, without necessarily explicitly specifying whether it is intracellular (in the context of digestion) or extracellular (circulating and detectable in plasma) in the tumor pathological setting.

For more clarity, the remainder of this article uses exclusively the name hPG80 to refer to extracellular progastrin.

A link between this protein and cancer has been known for more than 30 years[2]. hPG80 is involved in most of the biological functions that ensure the existence of cancer[3]. This peptide is secreted by tumor cells and found in the plasma of cancer patients from early stages[1]. It then has functions that are independent of digestion and totally different from progastrin and its only role as an intracellular precursor of gastrin.

Terminology[edit]

In the name hPG80, the "h" describes the human species: human; "PG" is a common script for the progastrin protein and the number 80 corresponds to the size of the protein: 80 amino acids.

The name hPG80 was thus proposed in the publication resulting from the work of Professor Benoît You under the management of Dominique Joubert and Alexandre Prieur[1] in order to remove ambiguities between the intracellular version of the protein (in the function of digestion) and its extracellular version of the protein (in the case of cancer patients) which is no longer, despite its name, the precursor of gastrin.  

Moreover, the existence of a phonetically identical peptide, the Pro-Gastrin Releasing Peptide (proGRP), accentuated a possible confusion around the name progastrin and the need for a specific name. It should be noted that, to date, more than half of the results resulting from the search for the word progastrin on search engines concern the proGRP and not the 80 amino acids molecule referred to the names progastrin and hPG80.

Chronology of scientific discoveries on hPG80[edit]

Figure 1: Timeline discribing key points of the link between hPG80 and cancer discovery

History[edit]

  • 1993 – 1994 : hPG80 is secreted by ovarian and colon cancer cells[4] · [5].
  • 1996 – 1997 : hPG80 is identified as necessary for the proliferation and tumorigenesis of colon cancer cells[6].
  • 2000 – 2001 : The GAST gene is a target of the ß-catenin/Tcf4 pathway[7]. hPG80 presence in colorectal cancer patient plasma is demonstrated[8].
  • 2005 : Ras and ß-catenin/Tcf4 pathways induce synergistic activation of the GAST gene, contributing to possible neoplastic progression[10].
  • 2007 : Inhibition of hPG80 expression inhibits the Wnt/ß-catenin pathway inducing decreased growth and tumor differentiation in intestinal tumor models[11].
  • 2012 : p53 gene mutation increases hPG80-dependent colonic proliferation and cancer formation[12].
  • 2015 : hPG80 is identified as a new pro-angiogenic factor[13].
  • 2016 : Autocrine secretion of hPG80 promotes survival and self-renewal of stem cells in colon cancer[14].
  • 2017 : The use of antibodies directed against hPG80 to target the Wnt pathway and cancer stem cells represents a new therapeutic track for cancer[15].
  • 2020 : hPG80 is detected in the plasma of patients with 11 different types of cancer. An association between longitudinal variations in hPG80 levels and anti-cancer treatments efficacy has been demonstrated[1].

Role in cancer[edit]

Through a variety of mechanisms, all crucial for tumor growth and survival, research has demonstrated the major role that hPG80 plays in tumor initiation and progression, generally using colorectal cancer as a model. Bardram was the first to hypothesize the presence of hPG80 in the early stages of the disease[2]. He evaluated the presence of hPG80 and its maturation products in the serum of patients with Zollinger-Ellison syndrome. This work showed that hPG80 measurement more accurately reflected tumor than the conventional measurement of amide gastrin. Indeed, hPG80 is more than 700 times more abundant than amide gastrin in colorectal tumors[16].

In the early 90s, it was shown that hPG80 was not fully matured in human colon cancer cell lines and, more importantly, that it was secreted by in vitro cultured cells[5]. These observations led to the study of autocrine and paracrine function of hPG80 in tumor cells[17]. Generally, it has been shown that hPG80 does not mature properly in cancer cells, particularly in colorectal cancer, because maturation enzymes are either absent or non-functional[4] · [5] · [18] · [19] · [20] · [16] · [21].

In 1996, it was demonstrated that GAST gene expression is required for human colon cancer cell tumorigenesis[6]. 60 to 80% of colon cancers express the GAST gene.

Through different experimental configurations, alteration of the GAST gene or neutralization of hPG80 resulted in a decrease in the number of tumors in mice with a tumor predisposition (mutation on the APC gene)[7] · [11] · [15]. Conversely, a significant increase in tumor formation was observed in mice overexpressing progastrin and treated with azoxymethane (AOM), a chemical carcinogen[22] · [23].

Pro-angiogenic factor[edit]

When a tumor develops, its need for oxygen and nutrients causes creation of new blood vessels. This process is called neo-angiogenesis. In 2015, hPG80 was shown to be a pro-angiogenic factor[13]. Indeed, hPG80 stimulates endothelial cells proliferation and migration and increases their ability to form capillary-like structures in vitro. Blocking the production of hPG80 (using shRNA) in xenograft cells in nude mice reduces tumor neovascularization.

Anti-apoptotic factor[edit]

Treatment of intestinal epithelial cells with hPG80 results in a significant loss of caspase 9 and caspase 3 activation and a decrease in DNA fragmentation. Therefore, hPG80 effect on cell survival results from both increased proliferation and decreased apoptosis[24].

Regulation of cell junctions[edit]

Cell migration is based on their ability to become independent of adjacent cells. Intercellular contacts integrity is essential for electrolyte uptake regulation as well as for tumor metastasis prevention. In 2003, it was demonstrated that blocking hPG80 secretion by an antisense construction directed against progastrin mRNA allows restoration of membrane localization of tight and adherent junctions constituent proteins in a human colorectal carcinoma cell line DLD-1[3]. hPG80 thus plays a role on cell contacts integrity.

Role in cancer stem cells[edit]

Cancer stem cells (CSCs) constitute a small proportion of the tumor, usually between 1 and 5%. But they are essential for tumor survival because they act as a "reactor". Giraud and al. have demonstrated the major role played by hPG80 in CSCs. These authors have shown that hPG80 expression is strongly increased in colorectal cancer cells cultured under conditions where CSCs are enriched[14]. They then showed that hPG80 was able to regulate CSCs frequency (survival and self-renewal) in vitro and in vivo. Subsequently, Prieur and al. demonstrated that when a neutralizing antibody is added to a cell culture or when human colorectal cancer cells implanted mice are treated in vivo with such an antibody, CSCs frequency is decreased in the same proportions[15]. These two scientific articles clearly show that hPG80 is a survival factor for CSCs. Moreover, hPG80 inhibition would induce CSC differentiation, opening the possibility of a differentiation therapy rather than a classical anti-proliferative therapy. Its main function is to help CSCs survive and spread to form metastasis, which probably explains why this peptide can be considered as a potential predictive marker for the presence of liver metastasis in colorectal cancer[25].

hPG80 and oncogenic signaling pathways[edit]

Wnt and K-Ras[edit]

Figure 2: hPG80, cornerstone in ongenetic pathways

The first event leading to colon cancer is in 80 to 90% of cases a constitutive activation of the Wnt/ß-catenin oncogenic pathway induced by mutations in the APC (Adenomatous polyposis coli) coding gene or the ß-catenin coding gene. Mutations induction into normal intestinal stem cells is sufficient to trigger tumorigenesis[26]. GAST gene which encodes hPG80 is activated by the Wnt oncogenic pathway. It is a downstream target of the ß-catenin/Tcf-4 signaling pathway[7].

Demonstration of the link between hPG80 and an oncogenic pathway has been described for K-Ras. Cell lines and colon cancer tissues with K-Ras mutations all had significantly higher levels of GAST mRNA than K-Ras wild type[27]. K-Ras effects on GAST expression are produced by activation of the Raf-MEK-ERK signal transduction pathway, final step being activation of the GAST gene promoter.

Since both K-Ras and the Wnt pathway induce GAST expression, the hypothesis of a possible cooperation between these two pathways to regulate hPG80 expression has been investigated[10]. Chakadar and al. found significant synergistic stimulation of the GAST gene promoter (by a factor of 25 to 40) by a combination of oncogenic ß-catenin and K-Ras overexpression. Activation of the GAST gene promoter was also shown to be dependent on other signalling signals: enhanced or suppressed by co-expression of wild-type SMAD4 or by a dominant negative mutant of SMAD4, respectively, and abrogated by inhibition of PI3K. Thus, constitutive activation of the Wnt pathway, considered to be at the onset of tumorigenesis in the colon, and the K-Ras oncogene, present in 50% of human colorectal tumors, synergistically stimulate the production of hPG80, a tumorigenesis promoter. Tumorigenesis induced by activation of the Wnt pathway is partially dependent on hPG80.

SRC, PI3K/Akt, NF-kB and Jak/Stat[edit]

The oncogene pp60 (c-Src) is activated in colon cancer cells and leads to increased amounts of hPG80[9]. This means that hPG80 production, which occurs during early tumorigenesis[11], could play a role in this activation, which is known as an early event in colon tumorigenesis[28] · [29]. The PI3K/Akt pathway, which is particularly involved in proliferation, is also activated by hPG80[11] · [30]. NF-kappaB is another important signaling messenger regulated by hPG80. Its involvement in mechanisms responsible for the anti-apoptotic effect of hPG80 has been demonstrated in pancreatic cancer cells in vitro[31] and in vivo in mice overexpressing the GAST gene[32]. JAK2 (Janus-activated kinase 2), STAT3 and kinases increases regulated by extracellular signals have also been observed in the colon mucosa of hGAS mice[30].

NOTCH[edit]

It has been shown that colon tumor cells which do not express hPG80 return to a 'normal' state'. This is due to the fact that when the Wnt pathway is inactivated, the JAG1 gene is repressed, inducing inactivation of the Notch pathway which plays a major role in the acquisition of a differentiated cell phenotype[33].

p-53[edit]

In 2012, the P53 gene mutation was shown to increase hPG80-dependent colon cells proliferation and colon cancer formation in mice[12].

hPG80 receptor[edit]

An identification of the hPG80 receptor has been the subject of several studies in recent years. However, hPG80 receptor identity remains a real issue in the scientific community. The receptor can activate a number of signaling pathways, either directly or indirectly, which is rather unusual for a receptor. This could indicate a peculiarity of this receptor and why it is difficult to identify it. The unidentified hPG80 receptor transduces a progastrin signal via various intracellular intermediates known to be involved in tumorigenesis.

High affinity binding sites have been described for the first time in intestinal epithelial cells using iodine recombinant human progastrin[34]. Affinity was in the range of 0.5-1 nM, which is receptor compatible. When biotinylated progastrin binding was evaluated by flow cytometry, strong and specific binding of progastrin to certain cell lines (IEC-6, IEC-18, HT-29, COLO320) was also detected[35]. A specificity of binding was confirmed by competition with cold, unlabelled hPG80, but not with carboxy-terminal glycine-containing gastrin or amidated gastrin-17. Binding was not influenced by the presence of the classical CCK-2 receptor.

It is clear from these two studies that there is a binding site/receptor for hPG80 that is distinct from binding to gastrin-17 amidated and to gastrin 17 with carboxy-terminal glycine (G17-Gly). The sequence of hPG80 interacting with this receptor is likely located in the last 26 amino acid residues of hPG80 carboxy-terminal end, which have been shown to be sufficient for its function[36]. However, this putative receptor identity is unknown.

One candidate is Annexin A2, identified as being able of binding progastrin and derived peptides[37]. Annexin A2 is a partial mediator of the effect of progastrin/gastrins. In particular, Annexin A2 mediates NF-kappaB upregulation and ß-catenin in response to progastrin in mice and HEK-293 cells[38]. In addition, annexin A2 may be involved in progastrin-dependent clathrin endocytosis. However, progastrin hPG80? affinity for Annexin A2 is not what would be expected for a specific receptor. And, although Annexin A2 plays a role in progastrin hPG80? functions, it does not fit a receptor function.

Another candidate is the G protein-coupled receptor 56 (GPCR56), expressed on both colon stem cells and cancer cells[39]. While human recombinant hPG80 promotes in vitro growth and survival of wild mice colon organoids, those from GPCR56-deficient mice (GPCR56-/-) are resistant to hPG80. However, although hPG80 has been shown to bind to cells expressing GPCR56, authors did not provide direct evidence of a hPG80 bound to GPCR56 itself. GPCR56 is a good candidate, but evidence that it is hPG80 receptor is to this day not established.

Clinical Applications[edit]

hPG80 through various mechanisms can be considered as a major promoter of tumorigenesis. hPG80 is found in the plasma of cancer patients and its neutralization induces tumor reversion.

Screening[edit]

Universal biomarker[edit]

Colorectal cancer is not the only type of cancer to express hPG80. Its expression has also been demonstrated in ovarian cancers[4], liver tumors[40] and also pancreatic tumors[41]. Thus, several types of tumors express the unmatured peptide.

hPG80 can be detected and quantified in the blood of cancer patients. A first demonstration has been made in colorectal cancer showing an increase of hPG80 and non-amide gastrin levels in plasma in these patients compared to a control series (healthy individuals)[8]. In addition, an hPG80 increase has been observed in patients with adenomatous polyps[15]. hPG80 is therefore expressed at all stages by the tumor, from early stages to metastasis.

Multi-cancer detection[edit]

hPG80 is found in different tumor types and secreted in vitro by several cancer cell types. A study has shown its presence in the blood of patients with 11 different cancers[1]: breast cancer, colorectal cancer, stomach/esophageal cancer, kidney cancer, liver cancer, non-small cell lung cancer, skin melanoma, ovarian cancer, pancreatic cancer, prostate cancer and uterine cancer (endometrial/cervical).

hPG80 in residual disease surveillance and response to therapy[edit]

Pre- and post-operative plasma assays of hPG80 in colorectal cancer patients show that hPG80 presence reflects tumor production[42].

It has been observed that hPG80 concentrations are increased in patients at risk of developing colorectal carcinoma[43]. Plus, an increase in hPG80 has been observed in hyperplastic polyps that have progressed to cancer[44] · [45].

hPG80 may also be a biomarker of liver metastasis in colorectal cancer[25].

In addition, You and al. observed a decrease in hPG80 levels after surgery in a patient cohort with gastrointestinal cancers with peritoneal involvement treated with post-operative chemotherapy and cytoreductive surgery[1].

Figure 3: Longitudinal changes in hPG80 and AFP levels during hepatocellular carcinoma management (inclusion; remission; progression) in a representative patient[1]

In addition, earlier detection of small lesions and monitoring of recurrence can be improved by measuring hPG80 levels as a complementary blood biomarker in a cohort of patients with hepatocellular carcinoma treated with local or systemic therapies [1](Fig. 3). Measured hPG80 levels are relevant in patients for whom alpha-fetoprotein (AFP) is below 20 ng/ml[46], an established threshold in clinical practice. Depending on disease management, patients in remission have lower levels of hPG80 than those in whom the cancer is still active.

Target to fight cancer[edit]

Antibody therapy[edit]

To date, no drug is able to target CSCs. Humanized anti-hPG80 antibodies[15], salone or in combination with chemotherapy, appears to be a promising approach. The use of anti-hPG80 antibodies has also been discussed as a potential treatment in colorectal cancer patients with a mutation in the KRAS gene. Targeting of hPG80 with the humanized anti-hPG80 antibody has been shown:

  • ua decrease in the self-renewal capacity of CSCs of various origins; 2. prolongation of in vitro and in vivo chemosensitivity and delayed relapse after treatment of T84 xenografted mouse cells; 3. decreased tumor burden and increased cell differentiation in the remaining tumors in transgenic mice developing Wnt-induced intestinal neoplasia.

This has recently been confirmed for ovarian, breast, esophageal, liver and gastric cancers [1] making this therapeutic antibody a potential multi-cancer drug.

Sensitization to radiotherapy[edit]

It has been shown that hPG80 is a radioresistant factor that can be targeted to sensitize rectal radiation-resistant cancers[47]. hPG80 decreased expression increases sensitivity to irradiation in colorectal cancer cell lines leading to increased radiation-induced DNA damage and apoptosis. In the same lineage, hPG80 targeting also results in radiation-induced survival pathways inhibition, Akt and ERK.

See also[edit]

Category:Tumor markers

References[edit]

  1. ^ a b c d e f g h i You Benoit, Frédéric Mercier, Eric Assenat, Carole Langlois-Jacques, Olivier Glehen; Julien Soulé, Léa Payen, Vahan Kepenekian, Marie Dupuy; Maud Flacelière, Philippe Elies, Fanny Belouin, Eric Morency, Véronique Saywell; Delphine Maucort-Boulch, Winston Tan, Pierre Liaud, Thibault Mazard; Glehen, Bérengère Vire, Laurent Villeneuve; Marc Ychoun, Manish Kohli, Dominique Joubert, Alexandre Prieur. "The oncogenic and druggable hPG80 (Progastrin) is overexpressed in multiple cancers and detected in the blood of patients". EBioMedicine. 51: 102574. doi:10.1016/j.ebiom.2019.11.035. PMC 6938867. PMID 31877416.{{cite journal}}: CS1 maint: PMC format (link) CS1 maint: multiple names: authors list (link)
  2. ^ a b c Bardram, L.; Hilsted, L.; Rehfeld, J. F. (1990-01-01). "Progastrin expression in mammalian pancreas". Proceedings of the National Academy of Sciences. 87 (1): 298–302. doi:10.1073/pnas.87.1.298. ISSN 0027-8424. PMC 53250. PMID 2296587.{{cite journal}}: CS1 maint: PMC format (link)
  3. ^ a b c Hollande, F. (2003-04-01). "Adherens junctions and tight junctions are regulated via different pathways by progastrin in epithelial cells". Journal of Cell Science. 116 (7): 1187–1197. doi:10.1242/jcs.00321.
  4. ^ a b c van Solinge, W. W.; Odum, L.; Rehfeld, J. F. (1993-04-15). "Ovarian cancers express and process progastrin". Cancer Research. 53 (8): 1823–1828. ISSN 0008-5472. PMID 8467501.
  5. ^ a b c Singh, P.; Xu, Z.; Dai, B.; Rajaraman, S.; Rubin, N.; Dhruva, B. (1994-03-01). "Incomplete processing of progastrin expressed by human colon cancer cells: role of noncarboxyamidated gastrins". American Journal of Physiology-Gastrointestinal and Liver Physiology. 266 (3): G459–G468. doi:10.1152/ajpgi.1994.266.3.G459. ISSN 0193-1857.
  6. ^ a b Singh, P.; Owlia, A.; Varro, A.; Dai, B.; Rajaraman, S.; Wood, T. (1996-09-15). "Gastrin gene expression is required for the proliferation and tumorigenicity of human colon cancer cells". Cancer Research. 56 (18): 4111–4115. ISSN 0008-5472. PMID 8797575.
  7. ^ a b c Koh, Theodore J; Chen, Duan. "Gastrin as a growth factor in the gastrointestinal tract". Regulatory Peptides. 93 (1–3): 37–44. doi:10.1016/S0167-0115(00)00176-2.
  8. ^ a b Siddheshwar, R. K.; Gray, J. C.; Kelly, S. B. (2003). "Plasma levels of progastrin but not amidated gastrin or glycine extended gastrin are elevated in patients with colorectal carcinoma". Gut. 48 (1): 47–52. doi:10.1136/gut.48.1.47. ISSN 0017-5749. PMC 1728168. PMID 11115822.
  9. ^ a b Brown, D.; Yallampalli, U.; Owlia, A.; Singh, P. (2003). "pp60 c-Src Kinase Mediates Growth Effects of the Full-Length Precursor Progastrin 1–80 Peptide on Rat Intestinal Epithelial Cells, in Vitro". Endocrinology. 144 (1): 201–211. doi:10.1210/en.2002-220501. ISSN 0013-7227.
  10. ^ a b Chakladar, Abhijit; Dubeykovskiy, Alexander; Wojtukiewicz, Lindsay J.; Pratap, Jitesh; Lei, Shi; Wang, Timothy C. (2005). "Synergistic activation of the murine gastrin promoter by oncogenic Ras and β-catenin involves SMAD recruitment". Biochemical and Biophysical Research Communications. 336 (1): 190–196. doi:10.1016/j.bbrc.2005.08.061.
  11. ^ a b c d Julie Pannequin, Nathalie Delaunay; Michael Buchert, Fanny Surrel; Jean–François Bourgaux, Joanne Ryan; Stéphanie Boireau, Jessica Coelho; André Pélegrin, Pomila Singh; Arthur Shulkes, Mildred Yim, Graham S Baldwin; Christine Pignodel, Gérard Lambeau, Philippe Jay; Joubert, Dominique; Hollande, Frédéric (2007). "β-Catenin/Tcf-4 Inhibition After Progastrin Targeting Reduces Growth and Drives Differentiation of Intestinal Tumors". Gastroenterology. 133 (5): 1554–1568. doi:10.1053/j.gastro.2007.08.023.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  12. ^ a b Ramanathan, Vigneshwaran; Jin, Guangchun; Westphalen, Christoph Benedikt; Whelan, Ashley; Dubeykovskiy, Alexander; Takaishi, Shigeo; Wang, Timothy C. (2012-04-26). "P53 Gene Mutation Increases Progastrin Dependent Colonic Proliferation and Colon Cancer Formation in Mice". Cancer Investigation. 30 (4): 275–286. doi:10.3109/07357907.2012.657814. ISSN 0735-7907. PMC 3697930. PMID 22480191.{{cite journal}}: CS1 maint: PMC format (link)
  13. ^ a b Najib, S; Kowalski-Chauvel, A; Do, C; Roche, S; Cohen-Jonathan-Moyal, E; Seva, C (2015). "Progastrin a new pro-angiogenic factor in colorectal cancer". Oncogene. 34 (24): 3120–3130. doi:10.1038/onc.2014.255. ISSN 0950-9232.
  14. ^ a b Giraud J., Failla L. M.; Pascussi J.-M., Lagerqvist E. L.; Ollier J., Finetti P.; Bertucci F., Ya C.; Imène Gasmi, Jean-François Bourgaux, Michel Prudhomme, Thibault Mazard; Imade Ait-Arsa, Leila Houhou, Daniel Birnbaum, André Pélegrin; Charles Vincent,, James G Ryall; Joubert, Dominique; Pannequin, Julie; Hollande, Francois (2016-06-15). "Autocrine Secretion of Progastrin Promotes the Survival and Self-Renewal of Colon Cancer Stem-like Cells". Cancer Research. 76 (12): 3618–3628. doi:10.1158/0008-5472.CAN-15-1497. ISSN 0008-5472.{{cite journal}}: CS1 maint: extra punctuation (link) CS1 maint: multiple names: authors list (link)
  15. ^ a b c d e Prieur Alexandre, Cappellini Monica; Habif Guillaume, Lefranc Marie-Paule; Mazard, Thibault; Morency Eric, Pascussi Jean-Marc; Flaceliere Maud, Cahuzac Nathalie, Berenger Vire; Durochat Amandine, Liaud Pierre, Ollier Jeremy; Pfeiffer Caroline, Poupeau Sophie, Saywell Veronique, Planque Chris; Assenat Eric, Bibeau Frederique; Bourgaux J.F., Pujol Pascal, Sezeur Alain; Ychou, Marc; Joubert, Dominique (2017-09-01). "Targeting the Wnt Pathway and Cancer Stem Cells with Anti-progastrin Humanized Antibodies as a Potential Treatment for K-RAS-Mutated Colorectal Cancer". Clinical Cancer Research. 23 (17): 5267–5280. doi:10.1158/1078-0432.CCR-17-0533. ISSN 1078-0432.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  16. ^ a b Kochman, Michael Lee; DelValle, John; Dickinson, Chris John; Boland, C.Richard (1992). "Post-translational processing of gastrin in neoplastic human colonic tissues". Biochemical and Biophysical Research Communications. 189 (2): 1165–1169. doi:10.1016/0006-291X(92)92326-S.
  17. ^ . Vol. 104. 1993-04. pp. 1099–1107. doi:10.1016/0016-5085(93)90279-L. {{cite news}}: Check date values in: |date= (help); External link in |lire en ligne= (help); Missing or empty |title= (help); Unknown parameter |nom1= ignored (|last1= suggested) (help); Unknown parameter |nom2= ignored (|last2= suggested) (help); Unknown parameter |nom3= ignored (|last3= suggested) (help); Unknown parameter |nom4= ignored (|last4= suggested) (help); Unknown parameter |prénom1= ignored (|first1= suggested) (help); Unknown parameter |prénom2= ignored (help)
  18. ^ Ciccotosto, Giuseppe D.; McLeish, Andrew; Hardy, Kenneth J.; Shulkes, Arthur (1995). "Expression, processing, and secretion of gastrin in patients with colorectal carcinoma". Gastroenterology. 109 (4): 1142–1153. doi:10.1016/0016-5085(95)90572-3.
  19. ^ Finley, G. G.; Koski, R. A.; Melhem, M. F.; Pipas, J. M.; Meisler, A. I. (1993-06-15). "Expression of the gastrin gene in the normal human colon and colorectal adenocarcinoma". Cancer Research. 53 (12): 2919–2926. ISSN 0008-5472. PMID 8504433.
  20. ^ Imdahl, A.; Mantamadiotis, T.; Eggstein, S.; Farthmann, E. H.; Baldwin, G. S. (1995-11-01). "Expression of gastrin, gastrin/CCK-B and gastrin/CCK-C receptors in human colorectal carcinomas". Journal of Cancer Research and Clinical Oncology. 121 (11): 661–666. doi:10.1007/BF01218524. ISSN 1432-1335.
  21. ^ Nemeth, J.; Taylor, B.; Pauwels, S.; Varro, A.; Dockray, G. J. (1993). "Identification of progastrin derived peptides in colorectal carcinoma extracts". Gut. 34 (1): 90–95. doi:10.1136/gut.34.1.90. ISSN 0017-5749. PMC 1374107. PMID 8432459.
  22. ^ Cobb, Stephanie; Wood, Thomas; Ceci, Jeffrey; Varro, Andrea; Velasco, Marco; Singh, Pomila (2004-03-15). "Intestinal expression of mutant and wild-type progastrin significantly increases colon carcinogenesis in response to azoxymethane in transgenic mice". Cancer. 100 (6): 1311–1323. doi:10.1002/cncr.20094. ISSN 0008-543X.
  23. ^ Singh, Pomila; Velasco, Marco; Given, Randall; Wargovich, Michael; Varro, Andrea; Wang, Timothy C. (2000-03-01). "Mice overexpressing progastrin are predisposed for developing aberrant colonic crypt foci in response to AOM". American Journal of Physiology-Gastrointestinal and Liver Physiology. 278 (3): G390–G399. doi:10.1152/ajpgi.2000.278.3.G390. ISSN 0193-1857.
  24. ^ Wu, Hai; Owlia, Azarmidokht; Singh, Pomila (2003). "Precursor peptide progastrin 1-80 reduces apoptosis of intestinal epithelial cells and upregulates cytochrome c oxidase Vb levels and synthesis of ATP". American Journal of Physiology-Gastrointestinal and Liver Physiology. 285 (6): G1097–G1110. doi:10.1152/ajpgi.00216.2003. ISSN 0193-1857.
  25. ^ a b Westwood, David A; Patel, Oneel; Christophi, Christopher; Shulkes, Arthur; Baldwin, Graham S (2017). "Progastrin: a potential predictive marker of liver metastasis in colorectal cancer". International Journal of Colorectal Disease. 32 (7): 1061–1064. doi:10.1007/s00384-017-2822-8. ISSN 0179-1958.
  26. ^ Huels, D J; Sansom, O J (2015). "Stem vs non-stem cell origin of colorectal cancer". British Journal of Cancer. 113 (1): 1–5. doi:10.1038/bjc.2015.214. ISSN 0007-0920. PMC 4647531. PMID 26110974.{{cite journal}}: CS1 maint: PMC format (link)
  27. ^ Nakata, H; Wang, S; Chung, D; Westwick, J; Tillotson, L (1998). "Oncogenic ras induces gastrin gene expression in colon cancer". Gastroenterology. 115 (5): 1144–1153. doi:10.1016/S0016-5085(98)70085-X.
  28. ^ Cartwright, C. A.; Meisler, A. I.; Eckhart, W. (1990-01-01). "Activation of the pp60c-src protein kinase is an early event in colonic carcinogenesis". Proceedings of the National Academy of Sciences. 87 (2): 558–562. doi:10.1073/pnas.87.2.558. ISSN 0027-8424. PMC 53304. PMID 2105487.{{cite journal}}: CS1 maint: PMC format (link)
  29. ^ Iravani, S.; Mao, W.; Fu, L.; Karl, R.; Yeatman, T.; Jove, R.; Coppola, D. (1998). "Elevated c-Src protein expression is an early event in colonic neoplasia". Laboratory Investigation; a Journal of Technical Methods and Pathology. 78 (3): 365–371. ISSN 0023-6837. PMID 9520949.
  30. ^ a b Ferrand, Audrey; Bertrand, Claudine; Portolan, Ghislaine; Cui, Guanglin; Carlson, Jane; Pradayrol, Lucien; Fourmy, Daniel; Dufresne, Marlene; Wang, Timothy C.; Seva, Catherine (2005-04-01). "Signaling pathways associated with colonic mucosa hyperproliferation in mice overexpressing gastrin precursors". Cancer Research. 65 (7): 2770–2777. doi:10.1158/0008-5472.CAN-04-0978. ISSN 0008-5472. PMID 15805277.
  31. ^ Rengifo-Cam, W.; Umar, S.; Sarkar, S.; Singh, P. (2007-08-01). "Antiapoptotic Effects of Progastrin on Pancreatic Cancer Cells Are Mediated by Sustained Activation of Nuclear Factor- B". Cancer Research. 67 (15): 7266–7274. doi:10.1158/0008-5472.CAN-07-1206. ISSN 0008-5472.
  32. ^ Umar, S; Sarkar, S; Cowey, S; Singh, P (2008). "Activation of NF-κB is required for mediating proliferative and antiapoptotic effects of progastrin on proximal colonic crypts of mice, in vivo". Oncogene. 27 (42): 5599–5611. doi:10.1038/onc.2008.169. ISSN 0950-9232. PMC 2891442. PMID 18521082.{{cite journal}}: CS1 maint: PMC format (link)
  33. ^ Pannequin, J.; Bonnans, C.; Delaunay, N.; Ryan, J.; Bourgaux, J.-F.; Joubert, D.; Hollande, F. (2009-08-01). "The Wnt Target Jagged-1 Mediates the Activation of Notch Signaling by Progastrin in Human Colorectal Cancer Cells". Cancer Research. 69 (15): 6065–6073. doi:10.1158/0008-5472.CAN-08-2409. ISSN 0008-5472.
  34. ^ Singh, P.; Lu, X.; Cobb, S.; Miller, B. T.; Tarasova, N.; Varro, A.; Owlia, A. (2003-02-01). "Progastrin 1–80 stimulates growth of intestinal epithelial cells in vitro via high-affinity binding sites". American Journal of Physiology-Gastrointestinal and Liver Physiology. 284 (2): G328–G339. doi:10.1152/ajpgi.00351.2002. ISSN 0193-1857.
  35. ^ Dubeykovskiy, Alexander; Nguyen, Thomas; Dubeykovskaya, Zinaida; Lei, Shi; Wang, Timothy C. (2008). "Flow cytometric detection of progastrin interaction with gastrointestinal cells". Regulatory Peptides. 151 (1–3): 106–114. doi:10.1016/j.regpep.2008.07.001. PMC 2630224. PMID 18674570.{{cite journal}}: CS1 maint: PMC format (link)
  36. ^ Ottewell, P. D.; Varro, A.; Dockray, G. J.; Kirton, C. M.; Watson, A. J. M.; Wang, T. C.; Dimaline, R.; Pritchard, D. M. (2005). "COOH-terminal 26-amino acid residues of progastrin are sufficient for stimulation of mitosis in murine colonic epithelium in vivo". American Journal of Physiology-Gastrointestinal and Liver Physiology. 288 (3): G541–G549. doi:10.1152/ajpgi.00268.2004. ISSN 0193-1857.
  37. ^ Singh, P; Wu, H; Clark, C; Owlia, A (2007). "Annexin II binds progastrin and gastrin-like peptides, and mediates growth factor effects of autocrine and exogenous gastrins on colon cancer and intestinal epithelial cells". Oncogene. 26 (3): 425–440. doi:10.1038/sj.onc.1209798. ISSN 0950-9232.
  38. ^ Sarkar, Shubhashish; Swiercz, Rafal; Kantara, Carla; Hajjar, Katherine A.; Singh, Pomila (2011). "Annexin A2 Mediates Up-regulation of NF-κB, β-catenin, and Stem Cell in Response to Progastrin in Mice and HEK-293 Cells". Gastroenterology. 140 (2): 583–595.e4. doi:10.1053/j.gastro.2010.08.054. PMC 3031715. PMID 20826156.{{cite journal}}: CS1 maint: PMC format (link)
  39. ^ Jin, Guangchun; Sakitani, Kosuke; Wang, Hongshan; Jin, Ying; Dubeykovskiy, Alexander; Worthley, Daniel L.; Tailor, Yagnesh; Wang, Timothy C. (2017-06-20). "The G-protein coupled receptor 56, expressed in colonic stem and cancer cells, binds progastrin to promote proliferation and carcinogenesis". Oncotarget. 8 (25): 40606–40619. doi:10.18632/oncotarget.16506. ISSN 1949-2553. PMC 5522213. PMID 28380450.{{cite journal}}: CS1 maint: PMC format (link)
  40. ^ Caplin, Martyn; Khan, Kosser; Savage, Kay; Rode, Jurgen; Varro, Andrea; Michaeli, Dov; Grimes, Stephen; Brett, Bernard; Pounder, Roy; Dhillon, Amar (1999). "Expression and processing of gastrin in hepatocellular carcinoma, fibrolamellar carcinoma and cholangiocarcinoma". Journal of Hepatology. 30 (3): 519–526. doi:10.1016/S0168-8278(99)80114-7.
  41. ^ Caplin, M.; Savage, K.; Khan, K.; Brett, B.; Rode, J.; Varro, A.; Dhillon, A. (2000-08-01). "Expression and processing of gastrin in pancreatic adenocarcinoma: Gastrin and pancreatic cancer". British Journal of Surgery. 87 (8): 1035–1040. doi:10.1046/j.1365-2168.2000.01488.x.
  42. ^ Konturek, Peter C.; Bielanski, Władysław; Konturek, Stanislaw J.; Hartwich, Artur; Pierzchalski, Piotr; Gonciarz, Macien; Marlicz, Krzysztof; Starzynska, Teresa; Zuchowicz, Monika; Darasz, Zbigniew; Götze, Jens P. (2002). "[No title found]". Digestive Diseases and Sciences. 47 (9): 1984–1991. doi:10.1023/A:1019652224424.
  43. ^ Paterson, Adrienne C; Macrae, Finlay A; Pizzey, Cathy; Baldwin, Graham S; Shulkes, Arthur (2014). "Circulating gastrin concentrations in patients at increased risk of developing colorectal carcinoma: Gastrins and colorectal carcinoma risk". Journal of Gastroenterology and Hepatology. 29 (3): 480–486. doi:10.1111/jgh.12417.
  44. ^ Do, Catherine; Bertrand, Claudine; Palasse, Julien; Delisle, Marie-Bernadette; Shulkes, Arthur; Cohen-Jonathan-Moyal, Elizabeth; Ferrand, Audrey; Seva, Catherine (2012). "A new biomarker that predicts colonic neoplasia outcome in patients with hyperplastic colonic polyps". Cancer Prevention Research (Philadelphia, Pa.). 5 (4): 675–684. doi:10.1158/1940-6207.CAPR-11-0408. ISSN 1940-6215. PMID 22366915.
  45. ^ Do, Catherine; Bertrand, Claudine; Palasse, Julien; Delisle, Marie-Bernadette; Cohen-Jonathan-Moyal, Elizabeth; Seva, Catherine (2013). "Activation of pro-oncogenic pathways in colorectal hyperplastic polyps". BMC Cancer. 13 (1): 531. doi:10.1186/1471-2407-13-531. ISSN 1471-2407. PMC 3829387. PMID 24209454.{{cite journal}}: CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link)
  46. ^ Sarwar, Shahid; Khan, Anwaar Ahmad; Tarique, Shandana (2014). "Validity of alpha fetoprotein for diagnosis of hepatocellular carcinoma in cirrhosis". Journal of the College of Physicians and Surgeons--Pakistan: JCPSP. 24 (1): 18–22. ISSN 1681-7168. PMID 24411536.
  47. ^ Kowalski-Chauvel, Aline; Gouaze-Andersson, Valerie; Vignolle-Vidoni, Alix; Delmas, Caroline; Toulas, Christine; Cohen-Jonathan-Moyal, Elizabeth; Seva, Catherine (2017-08-29). "Targeting progastrin enhances radiosensitization of colorectal cancer cells". Oncotarget. 8 (35): 58587–58600. doi:10.18632/oncotarget.17274. ISSN 1949-2553.
Retrieved from "https://en.wikipedia.org/w/index.php?title=User:Aarondeworld/sandbox&oldid=1104401712"