overview chan, timothy1, macaulay, calum2, lam, wan2, lam, stephen2, lonergan, kim2, ng, raymond2....

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Overview Chan, Timothy1, MacAulay, Calum2, Lam, Wan2 , Lam, Stephen2 , Lonergan, Kim2 , Ng, Raymond2. University of British Columbia, Vancouver, Canada BC Cancer Agency, Vancouver, Canada Objective The 5-year survival rate of an advanced lung cancer patient is only about 10%. If the cancer is caught early at the CIS (carcinoma in situ) stage, the 5-year survival rate is 90%. Currently, there are no studies have isolated biomarkers for this elusive CIS stage. We propose using lung SAGE data to isolate genes specific for CIS stages of lung cancer that are not present in bronchial metaplasia tissue. To find a set of candidate genes that are highly expressed in the CIS stages and lowly expressed in normal tissues, metaplasia tissues, and invasive tissues. To determine whether these genes are good candidate biomarkers from a biological stand point. To discover whether the expression level of these genes associated genes lead to the understanding of the inner workings of the early stages of the disease. Methodology To conduct our experiment we used 1 metaplasia library, 15 smoked-damaged (normal) libraries, 6 invasive libraries, and 5 CIS libraries. 27 SAGE PERMUTATION TEST PERMUTATION TEST CIS Normal CIS Invasive 79 Top 2000 Ranked Top 2000 Ranked Fold change of CIS/Normal average expression must be > 10 Fold change of CIS/Normal average expression must be > 5 Fold change of CIS/Metaplasia average expression must be > 2 Permutation score > 2.35 for both sets (p-value of 0.01) Results After applying the above criteria we obtained 18 tags. 14 had unigene ids and 11 mapped to genes with names. DSG3 0 20 40 60 80 100 120 140 Library Raw Gene Expression Top 18 Filtered Tags 0 20 40 60 80 100 120 140 160 180 200 Tag N am e R aw Expression C ount M et A vg C IS A vg IN V Avg DSC2 0 5 10 15 20 25 Library Raw GeneExpression 1.A calcium-dependent glycoprotein that is a member of the desmocollin subfmaily of the cadherin superfamily 2.Found primarily in epithelial cells where they constitute the adhesive proteins of the desmosome cell-cell junction anad are required for cell adhesion 1.A calcium-binding transmembrane glycoprotien component of desmosomes in vertebrate and epithelial cells. 2.A member of the cadherin cell adhesion molecule. Desmocollin 2 and desmoglein 3 are major components of cell adhesion molecules which play an important role in epithelial adhesion. Other desmosome families of the armadillo proteins (PKPs) and plakins were also found to be higher expressed (refer to boxplots). Squamous cell carcinoma cells overxpressing desmosomal cadherins have been shown to inhibit invasion. Future Directions Biological validation involving protein expression is required for our above hypothesis as SAGE only looks at the cell at the mRNA level. Analysis of other pathways involving the other set of genes need to done. It would be also interesting to look at the genes that are turned off or down-regulated in CIS stages but abundantly expressed in normal and invasive stages. Conclusion From our results we were unable to find a clear biomarker found that was exclusive to its tissue type (that is only found or produced by lung). Our study on the mRNA levels of the intercellular adhesion molecules suggest that when a squamous lung cell enters the early stages of lung cancer, adhesion genes are up regulated. As it enters the invasive stages, we hypothesize that these cancer cells have obtained the ability to obtain its own nutrients and thus do not need to anchor onto bronchial epithelial tissues. Interestingly, oral squamous cell carcinoma cells overexpressing desmosomal cadherins have been shown to inhibit invasion. *NOTE: pink box is the best mapped tag* Othere genes involved include ones involved in EGFR trafficking, phosphatase genes, and a tyrosine kinase receptors. All the genes were looked up on NCBI’s EST database to find where they are expressed. All these genes were found to be expressed in various tissues.

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Page 1: Overview Chan, Timothy1, MacAulay, Calum2, Lam, Wan2, Lam, Stephen2, Lonergan, Kim2, Ng, Raymond2. University of British Columbia, Vancouver, Canada BC

OverviewOverview

Chan, Timothy1, MacAulay, Calum2, Lam, Wan2 , Lam, Stephen2 , Lonergan, Kim2 , Ng, Raymond2.University of British Columbia, Vancouver, Canada

BC Cancer Agency, Vancouver, Canada

ObjectiveObjective

The 5-year survival rate of an advanced lung cancer patient is only about 10%.

If the cancer is caught early at the CIS (carcinoma in situ) stage, the 5-year survival rate is 90%.

Currently, there are no studies have isolated biomarkers for this elusive CIS stage.

We propose using lung SAGE data to isolate genes specific for CIS stages of lung cancer that are not present in bronchial metaplasia tissue.

To find a set of candidate genes that are highly expressed in the CIS stages and lowly expressed in normal tissues, metaplasia tissues, and invasive tissues.

To determine whether these genes are good candidate biomarkers from a biological stand point.

To discover whether the expression level of these genes associated genes lead to the understanding of the inner workings of the early stages of the disease.

MethodologyMethodologyTo conduct our experiment we used 1 metaplasia library, 15 smoked-damaged (normal) libraries, 6 invasive libraries, and 5 CIS libraries.

27 SAGE

PERMUTATION TEST PERMUTATION TEST

CIS Normal CIS Invasive

79

Top 2000 Ranked Top 2000 Ranked

Fold change of CIS/Normal average expression must be > 10

Fold change of CIS/Normal average expression must be > 5

Fold change of CIS/Metaplasia average expression must be > 2

Permutation score > 2.35 for both sets (p-value of 0.01)

ResultsResults After applying the above criteria we obtained 18 tags.

14 had unigene ids and 11 mapped to genes with names.

DSG3

0

20

40

60

80

100

120

140

Library

Raw

Gen

e Ex

pres

sion

Top 18 Filtered Tags

0

20

40

60

80

100

120

140

160

180

200

Tag Name

Raw

Exp

ress

ion

Co

un

t

Met Avg

CIS Avg

INV Avg

DSC2

0

5

10

15

20

25

Library

Raw

Gen

e Ex

pres

sion

1. A calcium-dependent glycoprotein that is a member of the desmocollin subfmaily of the cadherin superfamily

2. Found primarily in epithelial cells where they constitute the adhesive proteins of the desmosome cell-cell junction anad are required for cell adhesion

1. A calcium-binding transmembrane glycoprotien component of desmosomes in vertebrate and epithelial cells.

2. A member of the cadherin cell adhesion molecule.

Desmocollin 2 and desmoglein 3 are major components of cell adhesion molecules which play an important role in epithelial adhesion.

Other desmosome families of the armadillo proteins (PKPs) and plakins were also found to be higher expressed (refer to boxplots).

Squamous cell carcinoma cells overxpressing desmosomal cadherins have been shown to inhibit invasion.

Future DirectionsFuture Directions Biological validation involving protein expression is required for our above hypothesis as SAGE only looks at the cell at the mRNA level.

Analysis of other pathways involving the other set of genes need to done.

It would be also interesting to look at the genes that are turned off or down-regulated in CIS stages but abundantly expressed in normal and invasive stages.

ConclusionConclusion From our results we were unable to find a clear biomarker found that was exclusive to its tissue type (that is only found or produced by lung).

Our study on the mRNA levels of the intercellular adhesion molecules suggest that when a squamous lung cell enters the early stages of lung cancer, adhesion genes are up regulated.

As it enters the invasive stages, we hypothesize that these cancer cells have obtained the ability to obtain its own nutrients and thus do not need to anchor onto bronchial epithelial tissues.

Interestingly, oral squamous cell carcinoma cells overexpressing desmosomal cadherins have been shown to inhibit invasion.

*NOTE: pink box is the best mapped tag*

Othere genes involved include ones involved in EGFR trafficking, phosphatase genes, and a tyrosine kinase receptors.

All the genes were looked up on NCBI’s EST database to find where they are expressed. All these genes were found to be expressed in various tissues.